EP2395936A2 - Procédé de mise à disposition et de retraitement d'un produit médical, produit médical et système de mise en oeuvre du procédé - Google Patents

Procédé de mise à disposition et de retraitement d'un produit médical, produit médical et système de mise en oeuvre du procédé

Info

Publication number
EP2395936A2
EP2395936A2 EP10704507A EP10704507A EP2395936A2 EP 2395936 A2 EP2395936 A2 EP 2395936A2 EP 10704507 A EP10704507 A EP 10704507A EP 10704507 A EP10704507 A EP 10704507A EP 2395936 A2 EP2395936 A2 EP 2395936A2
Authority
EP
European Patent Office
Prior art keywords
packaging
user
medical
storage
medical product
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP10704507A
Other languages
German (de)
English (en)
Inventor
Robert Schrödel
Udo Simon
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Publication of EP2395936A2 publication Critical patent/EP2395936A2/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H40/00—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices
    • G16H40/20—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the management or administration of healthcare resources or facilities, e.g. managing hospital staff or surgery rooms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
    • A61B90/90—Identification means for patients or instruments, e.g. tags
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
    • A61B90/90—Identification means for patients or instruments, e.g. tags
    • A61B90/98—Identification means for patients or instruments, e.g. tags using electromagnetic means, e.g. transponders
    • G—PHYSICS
    • G06—COMPUTING; CALCULATING OR COUNTING
    • G06Q—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES; SYSTEMS OR METHODS SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES, NOT OTHERWISE PROVIDED FOR
    • G06Q10/00—Administration; Management
    • G06Q10/06—Resources, workflows, human or project management; Enterprise or organisation planning; Enterprise or organisation modelling
    • G—PHYSICS
    • G07—CHECKING-DEVICES
    • G07F—COIN-FREED OR LIKE APPARATUS
    • G07F17/00—Coin-freed apparatus for hiring articles; Coin-freed facilities or services
    • G07F17/0092—Coin-freed apparatus for hiring articles; Coin-freed facilities or services for assembling and dispensing of pharmaceutical articles
    • G—PHYSICS
    • G07—CHECKING-DEVICES
    • G07G—REGISTERING THE RECEIPT OF CASH, VALUABLES, OR TOKENS
    • G07G1/00—Cash registers
    • G07G1/0036—Checkout procedures
    • G07G1/0045—Checkout procedures with a code reader for reading of an identifying code of the article to be registered, e.g. barcode reader or radio-frequency identity [RFID] reader
    • G07G1/009—Checkout procedures with a code reader for reading of an identifying code of the article to be registered, e.g. barcode reader or radio-frequency identity [RFID] reader the reader being an RFID reader
    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H40/00—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices
    • G16H40/40—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the management of medical equipment or devices, e.g. scheduling maintenance or upgrades
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B50/00—Containers, covers, furniture or holders specially adapted for surgical or diagnostic appliances or instruments, e.g. sterile covers

Definitions

  • the present invention relates to a method for providing and reprocessing a medical product, e.g. a heart catheter according to the preamble of claim 1. Further, the present invention relates to a medical product according to the preamble of claim 15 and a system for carrying out the aforementioned method.
  • a medical product e.g. a heart catheter according to the preamble of claim 1.
  • the object of the present invention is to provide a novel method for the provision and reprocessing of a medical product, a corresponding medical product and a system for carrying out the method, whereby the aforementioned disadvantages can be avoided.
  • the above object is achieved in the generic method according to claim 1 by the following method steps:
  • steps (a) to (c) are performed in a pre-delivery organizational unit (13),
  • the method according to the invention makes it possible to carry out a completely documentable and monitorable sequence from the production or reprocessing of the medical product to its application and return to the weighing process. set up and error due to long service life, improper preparation and careless handling to avoid. Accidentally opened but unused medical products are identified and may be discarded. Medical products that require special reprocessing can be specifically directed to a special reprocessing process (eg sterilization process) using an automated process. Medical products, which are commonly provided as disposables, can be optimally reprocessed and reused with significant cost reductions.
  • a special reprocessing process eg sterilization process
  • such an ID is used, which is equipped with an additional data memory, so that in addition to the ID even more information can be stored together with the ID.
  • the packaging state of the medical product in the organizational unit e.g. at the manufacturer or wholesaler, and stored in a central file.
  • This file serves as a comparison file for decentralized files at the user.
  • a user-side storage space such as cardiac cabinet for cardiac catheterization
  • the storage and outsourcing of the medical product in question including its ID registered and transmitted to the organizational unit.
  • the organizational unit is thus informed about each filling and removal of the user-side storage bin.
  • the transmission of the ID of the medical product to the user-side storage location can expediently also be transmitted from the organizational unit to the user even before the medical product is sent or arrived. This ensures that transport-side damage can be detected immediately during storage.
  • the storage bin itself can be provided with an individual ID.
  • the respective ID of the storage bin is called up during storage of the medical product and also transmitted to the organizational unit. This results in an allocation of medical product to storage location, which is centrally documented.
  • the storage bin is typically z. For example, a cardiovascular cabinet or medical device cabinet in a specific clinic or practice.
  • the ID of the medical product can be conveniently realized by using an RFID tag with an individual address.
  • the medical article is expediently provided with an in particular captive RFID label with individually readable ID as well as additionally the packaging of the relevant medical article likewise with a further, in particular captive RJFID label with an individually readable ID.
  • the medical article thus retains a unique ID throughout its lifetime and thus can be identified at any time during the delivery and reprocessing operations.
  • the ID of the medical article and the ID of the associated package are the two units for generating the ID of the medical product as such. This ID is expediently changed, ie overwritten, during reprocessing of the medical product, so that the reprocessed product then has an independent new ID.
  • a cardiac catheter having a single reprocessing has a different ID than the original cardiac catheter.
  • the output ID can also be provided with additional information.
  • the ID of the medical product is provided with at least one product-related additional information, which should also be automatically readable.
  • product-related additional information which should also be automatically readable.
  • specific information can be provided to the medical product, which is compared with corresponding target information, in particular by the manufacturer or distributor and / or user.
  • certain documentation and / or warning and / or disabling functions may be provided, for example. be generated at the user's own storage bin.
  • a time stamp can be generated and preferably written in the ID of the medical product, so that it is recognized when the medical product is removed from the storage bin and possibly reused unused.
  • An import of the ID of the medical product at the user is expediently then when the storage space is closed. This has the advantage that without external impairment can be read multiple times and preferably a plausibility check can take place.
  • the ID of the medical article itself is expediently provided with readable additional information even with the number of additional reprocessing cycles (reprocessing cycles) and / or the expiry date and / or the code of the user and / or the code of the storage location.
  • the ID of the associated packaging is also provided, for example, with the number of permissible storage cycles and / or with the expiry date and / or the code of the user and / or with the packaging status information as readable additional information.
  • This additional information can be read, for example, in the medical record.
  • a desired separation point is expediently provided on the packaging, which is interrupted when the packaging is opened and the status of the ID is thereby changed, in particular the ID of the packaging is no longer legible.
  • This changed ID of the packaging can then be detected by a user-side scanning device. If the packaging of the medical article, for example a cardiac catheter after removal from e.g. the cardio cabinet is opened, the state of the ID of the packaging is thereby changed.
  • This status change is determined as information "packaging opened", preferably stored and / or passed on to the organizational unit.
  • the subject-matter of claim 13 has the advantage that a use of the medical article corresponding to the regulations can be ensured while largely excluding human error. For example, a warning and / or a disabling function is generated in the case of a cardiac catheter stored beyond the end of the expiration date.
  • the present invention further relates to a medical product according to the preamble of claim 16.
  • the medical article is provided with a captive RFID label with an individual, readable ID
  • the associated packaging likewise having a particular captive RFID label with individual, is provided readable ID and means for determining the packaging state "packaging still unopened” or "packaging open” are provided on the associated packaging.
  • This medical product makes it possible to be documented and identified at any time with regard to its condition and / or location during manufacture as well as at the user. Furthermore, certain warning and / or lock functions can be generated automatically. In addition, the medical product according to the invention also ensures increased security against counterfeiting.
  • the packaging may expediently have a desired separation point at the severance of the status of the RFID label of the packaging changes.
  • information is thus generated on the packaging-side ID which can be used to determine the packaging state "packaging still unopened” or "packaging opened".
  • the RFID tag thus ensures the identification of the packaging or the item. On the other hand, it also serves to determine the packaging condition.
  • a conductor track is provided for this purpose, the severity of which changes the status of the RFID label, in particular in the form of an altered induction current in the antenna coil of the RFID label.
  • the means for determining the state of packaging may be printed on a label to be affixed to the packaging, which label may conveniently contain other information as well. This is herstellurigstechnisch particularly favorable.
  • an RFID tag with a writable memory is used. This makes it possible to deposit additional information on the item side and / or on the packaging side, which are of particular importance in the case of reprocessing of the medical product.
  • the memory of the RFID tag is repeatedly writable. In this way, dependent on the reprocessing state dependent information can be updated on the RFID tag.
  • AIs transponders are expediently to use so-called passive transponders, which receive their energy exclusively by induction from the field of SchreiblsLesaku and even no energy storage, e.g. Batteries have. These are small and inexpensive.
  • the present invention relates to a system for carrying out the above-mentioned method, which is characterized for achieving the above object by the following features:
  • an organizational unit for providing medical products wherein the organizational unit comprises at least one writing and / or reading device for reading in the ID of the medical product and a superordinate memory,
  • the user-side storage space comprises at least one writing and / or reading device for writing and / or reading in the ID of the medical product, a memory and evaluation electronics, and
  • the system is subdivided into an organizational unit, for example a manufacturing company or a wholesaler, in which the medical items are first provided for distribution or reprocessed by the user after rewinding.
  • the organizational unit comprises at least one and / or reading means for reading and / or writing the ID of the medical product.
  • the read or overwritten information is collected and kept ready for a data comparison.
  • the system further includes a user-side storage space, in particular medical device Dispositions He example, in the case of a cardiac catheterization a cardiac cabinet in the clinic or in practice, in which at least one storage position is provided for an associated medical product.
  • the storage location also has a writing and / or reading device for writing and / or reading in the ID of the medical product as well as a memory and evaluation electronics.
  • data transmission means for example in the form of a radio transmission (public telephone network) or a transmission via data line (Internet, e-mail) are provided.
  • the storage space expediently has optical and / or acoustic warning devices and / or means for output blocking.
  • a reading device is provided in the storage area, which allows a determination of the packaging state of the packaging.
  • the present invention further includes, also claimed in a subordinate manner, a storage bin according to the preamble of claim 25.
  • the storage bin is characterized in that it comprises an RFID writing and / or reading unit. summarizes, has an evaluation and an interface can be provided by means of the data of the evaluation are exportable.
  • a particular embodiment of the storage space is closed by means of a door.
  • storage-side storage may alternatively be provided.
  • the storage-space-related data can also be stored in a paged-out storage which, for example, can be called up via an online access.
  • the storage space has a data port, by means of which the data of the storage space side memory or user-related memory to a separate storage medium such.
  • a data port by means of which the data of the storage space side memory or user-related memory to a separate storage medium such.
  • the storage / removal history can be issued and the hard copy, for example, the patient file supplied.
  • the RFID writing and / or reading unit is activated only when the door of the storage space is closed.
  • the radiation exposure is reduced to the bare minimum.
  • a monitoring system is preferably provided to close the doors automatically after a defined time window within which no movement takes place. Alternatively, this can also use a warning signal to alert the operator. 5
  • the display device ensures a user-friendly message in the event that a repeat order is necessary or has already been carried out automatically.
  • FIG. 1 is a greatly simplified schematic representation of an embodiment of a medical article
  • FIG. 2 shows a greatly simplified schematic representation of the medical product consisting of medical article and associated packaging, omitting the lid of the packaging;
  • Fig. 3 is an illustration of the lid of the package
  • FIG. 4 shows an illustration of the label to be applied to the lid of the packaging according to FIG. 3, containing the RFID label;
  • 5 shows a perspective view of the packaging with the label applied to the closed packaging;
  • FIG. 6 shows a perspective view of the packaging according to FIG. 5 in the opened state
  • Fig. 7 is a highly simplified schematic representation of the overall system for carrying out the method for the provision and reprocessing of a medical product and
  • FIG. 8 shows a greatly simplified schematic representation of a storage location for use in the system according to FIG. 7 once in the closed state (FIG. 8a) and in the opened state (FIG. 8b).
  • Reference numeral 1 in Fig. 1 denotes a medical article, for example, a so-called cardiac catheter or the like.
  • the medical article is captively connected to a RFID tag 2 having its own ID at a suitable location.
  • the RFID tag 2 includes an item-specific identification code or address as well as a memory for storing further additional data, such. As the number of additional reprocessing cycles and / or the expiration date and / or the user or recipient (clinic, practice) individualizing code.
  • the RFID tag 2 is a particularly passive transponder, which draws its energy from the field of the transmitting and / or reading unit by induction.
  • the memory is designed such that it can be described with data or existing data can be overwritten.
  • the subject medical device is sterilized for use and surrounded by a package 3.
  • the packaging 3 has expediently at the top a suspension 4 for user-side storage.
  • the packaging 3 is shown in Figure 2 without packaging lid.
  • the packaging lid comprises a stamped contour 6, which is intended to facilitate opening of the packaging 3 in the region of the packaging lid 5.
  • Fig. 4 shows a label which is applied to the top of the packaging lid 5 in the finished product.
  • the label 7 carries a packaging associated own RFID tag 9. Furthermore, the RFID tag 9 has a conductor 1 1, which is printed on the label 7.
  • the conductor track 11 is penetrated by a tear contour 10, at whose one end region a trigger tab 8 is provided.
  • the tear contour 10 is positioned on the label 7 such that it lies in the region of the central punched contour 6 of the packaging lid 5.
  • the label 7 can be used to inscribe information 12.
  • An overall illustration of the packaging 3, the packaging-side punched contour 6 and the label 7 can be seen in FIG.
  • the medical product consisting of the medical article 1 including its packaging 3, comes into circulation.
  • the info description may include indications of the expiration date, the number of reprocessing cycles already passed, and information regarding the recipient.
  • the RFID label 9 ensures a firmly defined electromagnetic status A.
  • the tab 8 of the label is taken and pulled down. 5) and the electromagnetic status A of the RFID tag 9 changes to the status B ("package opened") the packaging cover is to open outwards in the manner of a double door, as shown in Fig. 6.
  • the memory of the RFID label 9 of the packaging may also contain additional information, such as expiry date, information about the recipient (clinic, practice). This information is also already registered by the manufacturer. This information is also not overwritten. However, the receiver information may be overwritten by the remanufacturer if necessary.
  • FIG. 7 now shows the system according to the invention for carrying out the method according to the invention.
  • the system includes an organizational unit 13 prior to delivery, for example, a manufacturing facility or a reprocessing facility having at least one dedicated RFID read and / or write unit 21.
  • the system further includes an area of the user 20, such as a clinic or surgery.
  • a storage space 15 for example in the form of a cardiovascular cabinet or other cabinets for medical items.
  • the storage space 15 has several storage positions, each of which is associated with a medical product consisting of medical article 1 and packaging 3. In the case of FIG. 7, there are a total of seven.
  • the campground 15
  • the storage space 15 and / or its storage positions is or are provided with its own ID or own ID 's, expediently in the form of RFID labels.
  • the storage space 15 and / or its storage positions can be provided with an ID that has already been allocated, in particular system-integrated.
  • the storage space 15 has a (not shown) door, at least one RFID write and / or read unit 22 and an evaluation 16 and receiving antenna 17.
  • the transmitter 16 has a user-side memory 24.
  • a user-related memory 24a which is not on-site at the user, for example, a server-based memory, be provided.
  • the organizational unit 13 also has an antenna 14.
  • the organization unit 13 and the storage location 15 can be connected via a data line (Internet, intranet or the like).
  • a voice control for example, to ensure a voice-controlled opening or closing the door.
  • a medical article 1 of the type according to, for example, FIG. 1 is provided with an RFID tag 2.
  • the memory of the RFID tag 2 by an RFID writing and / or reading unit 21 with the additional
  • a package 3 including a label according to FIG. 4 is created.
  • the packaging is provided with its own RFID tag 9 with its own ID.
  • the memory of the RPID label 9 of the packaging 3 contains, in addition to the individual ID, an indication of the expiry date as well as information regarding the recipient as well as information about the organizational unit 13 (address, etc.).
  • the individual ID and the expiration date including the information about the recipient are also applied in the area of the organizational unit 13.
  • the finished product according to FIG. 5 is delivered to the user 20 and introduced there into the storage space 15.
  • the ID unit 9 of the packaging is read out from the R-FID writing and / or reading unit 22 when the medical product is placed in the storage location 15 at the storage location 15 selected for this purpose, and via the radio link 18 or the data line 19 is transmitted to the organizational unit 13.
  • an encoding of the storage space 15 or of the storage space 15 including the storage location within the same is transmitted. stand-alone save synced information.
  • the specialist opens the storage location 15, this justifies an audible signal if necessary. At the same time the
  • the RFID read / write device 22 recognizes the change in state of the transponder, stores it likewise in the user-side memory of the evaluation electronics 16 and additionally transmits the information to the organizational unit 13. In this case, after data synchronization both in the memory of the organizational unit 13 and in the memory of the transmitter 16 at the user the information "packaging open".
  • the medical article 1 After use of the medical article 1, it is again accommodated in the packaging 3 and sent back to the organizational unit 13. In this case, it is checked by the RFID read / write device 21 provided there, identified and fed to the reprocessing process. After this has taken place, the medical article 1 is repackaged in a new package 3 to make a new label 7 and a new ID of the (remanufactured) medical product is made from the ID of the medical article in conjunction with the ID of the new package , At the same time, only the number 9 and a corresponding expiry date are indicated on the label 7 with regard to the number of permissible reprocessing cycles. The original identification data can be overwritten here.
  • the reprocessed medical product is transmitted to the user 20 and stored again in the storage space 15.
  • the RFID read / write device 22 recognizes to the user 20 that it is a reprocessed product, that the ID of the medical article has already been read in one pass. had been registered. In the event that this is a correctly reprocessed product, which is detected by the synchronization of the databases, the possibly existing original identification code group will be overwritten by the new one.
  • the RFID tag 2 of the relevant medical article 1 has been provided with a time stamp, it can be checked for re-storage with regard to a possible expiration date during storage of the product outside the storage unit and this be acknowledged by a corresponding warning message or a warning tone.
  • the new time stamp is stored in the database of the storage unit. In this case, it can be taken into account whether the permissible period of time for the storage of the product with the packaging (s) is absolute or should be reset at each re-storage. This avoids that an already opened medical article 1 is inadvertently not used for a long time and is therefore exposed to possible contamination.
  • a corresponding RF ID writing and / or reading unit 22 can therefore be provided directly on the operating table or treatment table.
  • the time stamp may merely be deposited, for example, via time recording provided in the user-side part of the system, without that information being written into the RFID tag of the medical article 1 or the packaging in question.
  • the RFID label of the medical product and the RFID label of the packaging with different frequencies, for example the RFID label of the medical 13.56 MHz object and the RFID tag of the packaging with a low frequency in the range of 30 - 500 kHz. This ensures that only the RFID tag of the medical article or the RFID label of the package is queried, identified and possibly also described in the query.
  • FIGS. 8a and 8b show an expedient embodiment of the storage space 15 once in the closed state (FIG. 8a) and in the open state (FIG. 8b).
  • the storage space has a closable by means of a door 30 space. It has a user-side memory 24 or, alternatively, a user-related memory 24a, an evaluation electronics 16 and antenna 17.
  • the evaluation electronics 16 is connected via a storage-site-side printer 26 for outputting protocols and the like.
  • a display 28 and a data port for reading or reading certain data is provided on the front side of the storage space 15, a display 28 and a data port for reading or reading certain data is provided.
  • an externally accessible interface 31 for data export and / or import It may expediently be a usual standardized 4.000steüe such. B. USB etc. act.
  • the storage bin 15 has a warning device 32, which outputs a visual and / or audible warning if necessary.
  • a movement sensor 29 is arranged, with which can be detected when a removal movement or insertion movement has taken place.
  • the device 27 for controlling the door 30 is first actuated, for example, by a voice command of the operator and the door 30 is opened.
  • storage bin 15 Within storage bin 15 are RFID writing and / or reading units with which the respective IDs of the medical products are identified and possibly overwritten.
  • the present invention makes it possible to provide a medical product, which is subjected to a reprocessing process, with increased safety at a reduced documentation cost.
  • the present invention therefore represents a very significant contribution in the relevant field of technology.

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Abstract

L'invention concerne un procédé de mise à disposition, en particulier de mise à disposition et de retraitement d'un produit médical, comprenant un objet médical, par exemple un instrument médical, qui est conservé dans un emballage, en particulier de manière stérile, et qui est remis à son utilisateur dans cet état. Le procédé est caractérisé par les étapes suivantes : attribution d'un identificateur individuel au produit médical, équipement de l'emballage de l'objet médical d'un dispositif permettant de constater l'état de l'emballage, à savoir « emballage non ouvert » ou « emballage ouvert », lecture de l'identificateur du produit médical et sauvegarde de l'identificateur dans une mémoire hiérarchiquement supérieure, les étapes (a) à (c) étant exécutées par une unité organisationnelle (13) située avant la livraison, mise à disposition du produit médical à l'utilisateur par l'unité organisationnelle (13), constatation de l'identificateur du produit médical en liaison avec l'utilisateur, en particulier du côté de l'utilisateur, et sauvegarde de l'identificateur dans une mémoire liée à l'utilisateur, en particulier du côté de l'utilisateur, comparaison des données liées à l'utilisateur avec les données présentes dans la mémoire hiérarchiquement supérieure.
EP10704507A 2009-02-13 2010-02-09 Procédé de mise à disposition et de retraitement d'un produit médical, produit médical et système de mise en oeuvre du procédé Withdrawn EP2395936A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102009008917A DE102009008917A1 (de) 2009-02-13 2009-02-13 Verfahren zur Zurverfügungstellung und Wiederaufbereitung eines medizinischen Produkts, medizinisches Produkt sowie System zur Durchführung des Verfahrens
PCT/EP2010/000790 WO2010091838A2 (fr) 2009-02-13 2010-02-09 Procédé de mise à disposition et de retraitement d'un produit médical, produit médical et système de mise en œuvre du procédé

Publications (1)

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EP2395936A2 true EP2395936A2 (fr) 2011-12-21

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EP10704507A Withdrawn EP2395936A2 (fr) 2009-02-13 2010-02-09 Procédé de mise à disposition et de retraitement d'un produit médical, produit médical et système de mise en oeuvre du procédé

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US7564354B2 (en) * 2005-12-29 2009-07-21 International Business Machines Corporation Monitoring device for detecting opening of packaging
WO2008033574A2 (fr) * 2006-09-13 2008-03-20 Clearcount Medical Solutions, Inc. appareil et procédés pour surveiller des objets dans un champ chirurgical
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WO2010091838A3 (fr) 2010-11-11
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