CN112561012A - Identification coding method for medical instrument - Google Patents
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- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06K—GRAPHICAL DATA READING; PRESENTATION OF DATA; RECORD CARRIERS; HANDLING RECORD CARRIERS
- G06K19/00—Record carriers for use with machines and with at least a part designed to carry digital markings
- G06K19/06—Record carriers for use with machines and with at least a part designed to carry digital markings characterised by the kind of the digital marking, e.g. shape, nature, code
- G06K19/06009—Record carriers for use with machines and with at least a part designed to carry digital markings characterised by the kind of the digital marking, e.g. shape, nature, code with optically detectable marking
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- 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
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- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06K—GRAPHICAL DATA READING; PRESENTATION OF DATA; RECORD CARRIERS; HANDLING RECORD CARRIERS
- G06K19/00—Record carriers for use with machines and with at least a part designed to carry digital markings
- G06K19/06—Record carriers for use with machines and with at least a part designed to carry digital markings characterised by the kind of the digital marking, e.g. shape, nature, code
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Abstract
The invention requests to protect an identification coding method for a medical instrument, which comprises the following steps: u1, identifying and coding raw materials required by the production of medical equipment and equipment, and uploading the raw materials to an enterprise database; u2, marking production information of machinery, operators, production processes and the like of a production line; u3, marking the identification codes of the materials, production processes, products and the like which are marked by codes through carriers such as two-dimensional codes, bar codes, RFID and the like, and recording the data of the raw materials, the production processes and the products in the whole life cycle through related identification technologies; u4, according to the code sign of product, carry out the sign analysis to it, obtain the full life cycle information of product to be favorable to product traceability, quality management and control and product supervision. The invention realizes the identification of the medical appliance industry from the whole life cycle of materials, finished products, after sales and the like, thereby realizing the functions of product traceability, quality control and production supervision.
Description
Technical Field
The invention belongs to the field of image processing, and particularly relates to an image restoration technology.
Background
The product identification of medical equipment products has extremely important reuse. By carrying out identification coding on the medical apparatus, the integration and sharing of supervision data are facilitated, the full life cycle management of the medical apparatus is enhanced, the combination of government supervision and social management is realized, the situation of social co-management is formed, and the transformation, upgrading and health development of the industry are assisted. Each medical apparatus and instrument is endowed with a unique identifier, so that the medical apparatus and instrument has a unique ID, the management and supervision of product information can be realized, and related product information services are obtained by inquiring the identifier information through a national industrial Internet identifier analysis platform constructed in China.
The coding used by the traditional medical instrument product is a private coding mode in an enterprise, conflicts exist in circulation and use, the problems that a unified platform cannot be used for analysis and the like exist, the coding modes are not unified, and effective supervision is difficult to form.
Disclosure of Invention
The present invention is directed to solving the above problems of the prior art. An identification coding method for a medical instrument is proposed. The technical scheme of the invention is as follows:
an identification coding method for a medical instrument, comprising the steps of:
u1, identifying and collecting the information of the raw material: in the production field of medical instruments, carrying out one-to-one corresponding identification coding on raw materials, production machine numbers and operators entering a production line, recording the processing and processing procedures of the raw materials and the operators of the products through corresponding machines, and transmitting the identification data to an internal storage system of an enterprise by carrying out identification data acquisition on the production field;
u2, through one or a combination of several modes including image recognition, wireless sensing and RFID, carrying out material information acquisition, production machine information acquisition and medical instrument finished product information acquisition on a medical instrument production field; for the produced medical appliance products, carrying out enterprise internal coding on product attribute information including product specification models, batches and single products, carrying out coding mapping through an enterprise identification analysis node, collecting in the step U1 in a wired and wireless transmission mode by using multiple modes such as two-dimensional code identification, bar code identification, RFID and the like, forming a mapping relation between the collected identification data and the product identification to form a unique universal identification, and uploading the unique universal identification to an enterprise node identification analysis system for identification registration and filing storage;
u3, heterogeneous coding unification step: when each medical equipment production enterprise produces a product, an internal coding system is used, under the condition that the internal coding system is not changed, after the medical equipment production enterprise finishes product coding, product identification information and product attribute information are uploaded to a medical equipment industry identification analysis secondary node for registration, the secondary node is audited, after the audit is passed, the product is coded according to the unique coding of the product in a secondary node coding mode, and the secondary node uploads the audited identification to the top level node of the country;
and U4, the user enters an identification analysis system to analyze according to the product identification to obtain product data.
Further, the specific steps of the medical instrument identification code in step U2 are as follows:
(1) coding important attribute information related to the production process including raw material purchase, outside service supply, factory inspection, warehouse management, component production, process matching, process inspection, whole machine assembly, delivery inspection, finished product inventory, sales order, installation and debugging and maintenance service, and recording a coding system of internal specifications of an enterprise for the material supplier and the material production date;
(2) after the raw material is processed, recording a minimum processing unit, a corresponding batch and a processing machine, simultaneously recording the information of workers who operate, and uniformly identifying codes in the processing procedure;
(3) performing quality detection and sample submission on the processed product, marking the product after the quality detection is qualified, and accurately coding the product to product specification, batch and single product according to the supervision requirement of the national drug administration on medical instruments;
(4) the enterprise uploads the coded product to a second-level node for medical instrument identifier analysis, the second-level node reports the product to a national drug administration for registration and filing, after the product passes the audit, the second-level node reports the product to a national top-level node for audit, after the product passes the top-level audit, the product is filed and stored, identifier registration is completed, and the identifier takes effect formally.
Further, the specific steps of compatibility and unification of heterogeneous codes in the step U3 are as follows:
(1) before accessing the secondary node, the material coding and the product coding of an enterprise in production are carried out according to a private coding mode inside the enterprise, and meanwhile, after the enterprise accesses the secondary node, the enterprise assigns codes inside the enterprise by adopting a coding system of a secondary node identification analysis system;
(2) before accessing a secondary node, an enterprise needs to register an enterprise identification prefix in the secondary node, wherein the enterprise identification prefix is used as a unique ID of the enterprise in an industrial internet identification analysis system;
(3) the enterprise registers the coded product information in a secondary node, the secondary node reports the product information reported by the enterprise to the national drug administration for registration and filing, the national drug administration returns the product information to the secondary node after approval, the secondary node reports the product information to a national top node, the top node registers the product information after passing, and the secondary node stores the product information by feeding back the result to the secondary node;
(4) when the enterprise uploads product information to the secondary node. The secondary node performs uniqueness assignment on the self-defined code of the product enterprise according to a code system, and codes the product in a mode of unique identification prefix and product identification suffix, so that the unique identification code of the product is completed;
(5) by means of the method of identifying the prefix and the product suffix, the unification of heterogeneous codes among enterprises is completed.
Further, in step U4, the enterprise user of the identifier resolution system may use a self-established identifier resolution server or use a secondary node identifier resolution hosting manner to implement resolution of the product information. When the self-built identification analysis server carries out identification registration filling information, the IP address and the port number corresponding to the identification analysis server and an interface for identification analysis need to be uploaded, and when the secondary node receives the identification analysis, the secondary node carries out request forwarding to a specified interface. By using a secondary node hosting mode, detailed information of the identifier needs to be uploaded to a secondary node for identifier information registration, so that the secondary node completes identifier analysis work when receiving an analysis request.
The invention has the following advantages and beneficial effects:
the invention provides a method for identifying and coding industrial Internet medical instrument industry, which has the following remarkable effects:
(1) by using the identification coding method, detailed records are carried out from the whole life cycle processes of production raw materials, production process, process information, product information, after-sale information and the like of the medical instrument, the whole process tracing of the medical instrument product is realized, the identification coding method is an important hand grip for the innovation of the medical instrument supervision means and the promotion of the supervision efficiency, and the identification coding method plays a positive role in strictly guarding the safety bottom line of the medical instrument and the high-quality development of the power-assisted medical instrument industry.
(2) By establishing the medical instrument identification analysis system, the integration and sharing of supervision data are facilitated, a supervision mode is innovated, the supervision efficiency is improved, the full life cycle management of the medical instrument is enhanced, the market is purified, the operator environment is optimized, the government supervision and the social management are combined, the situation of social co-management is formed, the production transformation upgrading and the health development are assisted, safer and more efficient medical services are provided for the public, and the feeling of acquisition of people is enhanced.
(3) Through unified sign to medical instrument, realized mutual compatibility between the heterogeneous code, be favorable to the state supervise pipe to carry out market supervision, also promote simultaneously that supply chain is in coordination between the enterprise, the accurate butt joint of sharization manufacturing and enterprise's production system, product full life cycle management and intelligent service.
Drawings
FIG. 1 is a flow chart of an identification coding method for a medical instrument according to a preferred embodiment of the present invention;
FIG. 2 is a schematic diagram of medical device identification information registration;
fig. 3 is a flowchart of medical device identifier resolution.
Detailed Description
The technical solutions in the embodiments of the present invention will be described in detail and clearly with reference to the accompanying drawings. The described embodiments are only some of the embodiments of the present invention.
The technical scheme for solving the technical problems is as follows:
as shown in fig. 1, a flow chart for implementing the present invention includes the following steps:
u1, identifying and collecting the information of the raw material: in the production field of medical instruments, carrying out one-to-one corresponding identification coding on raw materials, production machine numbers and operators entering a production line, recording the processing and processing procedures of the raw materials and the operators of the products through corresponding machines, and transmitting the identification data to an internal storage system of an enterprise by carrying out identification data acquisition on the production field;
u2, detailing the specifications, the batches and the single products of the produced medical appliance products, carrying out enterprise internal coding according to corresponding product attribute information, carrying out coding mapping through an enterprise identification analysis node, mapping the data acquired in the step U1 to a product identification to form a unique universal identification, and uploading the unique universal identification to an enterprise node identification analysis system for identification registration and record storage;
u3, heterogeneous coding unification: when each medical equipment production enterprise produces products, the internal coding system is used, under the condition that the internal coding system is not changed, after the medical equipment production enterprise finishes product coding, product identification information and product attribute information are uploaded to a medical equipment industry identification analysis secondary node for registration, the secondary node is audited, and after the audit is passed, the product is uniquely coded according to a secondary node coding mode to assign codes to the product. The secondary node uploads the identifier passing the audit to a national top node;
and U4, the user enters an identification analysis system to analyze according to the product identification to obtain product data. Regarding identification analysis, an enterprise user can analyze product information by using a self-built identification analysis server or by using a secondary node identification analysis hosting mode.
Preferably, as shown in fig. 2, the specific steps of the medical device identification code are as follows:
coding important attribute information related to production processes such as raw material purchase, outside service supply, factory inspection, warehouse management, component production, process matching, process inspection, whole machine assembly, delivery inspection, finished product inventory, sales order, installation and debugging, maintenance service and the like, for example, recording a coding system of internal specifications of an enterprise by a material supplier and a material production date;
after the raw material is processed, recording a minimum processing unit, a corresponding batch and a processing machine, simultaneously recording the information of workers who operate, and uniformly identifying codes in the processing procedure;
quality detection and sample inspection are carried out on the product formed after processing, the product is endowed with a code mark when the quality detection is qualified, and the product code is accurate to the product specification, batch and single product according to the supervision requirement of the national drug administration on medical instruments.
(5) The enterprise uploads the coded product to a second-level node for medical instrument identifier analysis, the second-level node reports the product to a national drug administration for registration and filing, after the product passes the audit, the second-level node reports the product to a national top-level node for audit, after the product passes the top-level audit, the product is filed and stored, identifier registration is completed, and the identifier takes effect formally.
As shown in fig. 2, preferably, the specific steps of the heterogeneous coding compatibility unification are as follows:
(1) before accessing the secondary node, the material coding and the product coding of an enterprise in production are carried out according to a private coding mode inside the enterprise, and meanwhile, after the enterprise accesses the secondary node, the enterprise can assign codes inside the enterprise by adopting a coding system of a secondary node identification and analysis system;
(2) before accessing a secondary node, an enterprise needs to register an enterprise identification prefix in the secondary node, wherein the enterprise identification prefix is used as a unique ID of the enterprise in an industrial internet identification analysis system;
(3) the enterprise registers the coded product information in a secondary node, the secondary node reports the product information reported by the enterprise to the national drug administration for registration and filing, the national drug administration returns the product information to the secondary node after approval, the secondary node reports the product information to a national top node, the top node registers the product information after passing, and the secondary node stores the product information by feeding back the result to the secondary node;
(4) when the enterprise uploads product information to the secondary node. The secondary node assigns uniqueness to the self-defined code of the product enterprise according to a code system, and codes the product in a mode of unique identification prefix and product identification suffix, so that the unique identification code of the product is completed.
(5) By means of the method of identifying the prefix and the product suffix, the unification of heterogeneous codes among enterprises is completed.
The method illustrated in the above embodiments may be implemented by a computer chip or an entity, or by a product with certain functions. One typical implementation device is a computer. In particular, the computer may be, for example, a personal computer, a laptop computer, a cellular telephone, a camera phone, a smartphone, a personal digital assistant, a media player, a navigation device, an email device, a game console, a tablet computer, a wearable device, or a combination of any of these devices.
Computer-readable media, including both non-transitory and non-transitory, removable and non-removable media, may implement the information storage by any method or technology. The information may be computer readable instructions, data structures, modules of a program, or other data. Examples of computer storage media include, but are not limited to, phase change memory (PRAM), Static Random Access Memory (SRAM), Dynamic Random Access Memory (DRAM), other types of Random Access Memory (RAM), Read Only Memory (ROM), Electrically Erasable Programmable Read Only Memory (EEPROM), flash memory or other memory technology, compact disc read only memory (CD-ROM), Digital Versatile Discs (DVD) or other optical storage, magnetic cassettes, magnetic tape magnetic disk storage or other magnetic storage devices, or any other non-transmission medium that can be used to store information that can be accessed by a computing device. As defined herein, a computer readable medium does not include a transitory computer readable medium such as a modulated data signal and a carrier wave.
It should also be noted that the terms "comprises," "comprising," or any other variation thereof, are intended to cover a non-exclusive inclusion, such that a process, method, article, or apparatus that comprises a list of elements does not include only those elements but may include other elements not expressly listed or inherent to such process, method, article, or apparatus. Without further limitation, an element defined by the phrase "comprising an … …" does not exclude the presence of other like elements in a process, method, article, or apparatus that comprises the element.
The above examples are to be construed as merely illustrative and not limitative of the remainder of the disclosure. After reading the description of the invention, the skilled person can make various changes or modifications to the invention, and these equivalent changes and modifications also fall into the scope of the invention defined by the claims.
Claims (4)
1. An identification coding method for a medical instrument, characterized by comprising the following steps:
u1, identifying and collecting the information of the raw material: in the production field of medical instruments, carrying out one-to-one corresponding identification coding on raw materials, production machine numbers and operators entering a production line, recording the processing and processing procedures of the products from the raw materials through corresponding machines and specific operators, and transmitting the products to an internal storage system of an enterprise by carrying out identification data acquisition on the production field;
u2, through one or a combination of several modes including image recognition, wireless sensing and RFID, carrying out material information acquisition, production machine information acquisition and medical instrument finished product information acquisition on the production field of the medical instrument; for the produced medical appliance products, product attribute information including product specification models, batches and single products is subjected to enterprise internal coding, coding mapping is carried out through an enterprise identification analysis node, collected identification data is mapped to product identifications in multiple modes including two-dimensional code identification, bar code identification and RFID in the step U1 through wired and wireless transmission modes, unique universal identifications are formed, and the unique universal identifications are uploaded to an enterprise node identification analysis system for identification registration and record storage;
u3, heterogeneous coding unification step: when each medical equipment production enterprise produces a product, an internal coding system is used, under the condition that the internal coding system is not changed, after the medical equipment production enterprise finishes product coding, product identification information and product attribute information are uploaded to a medical equipment industry identification analysis secondary node for registration, the secondary node is audited, after the audit is passed, the product is coded uniquely according to a secondary node coding mode, and the secondary node uploads the audited identification to a national top node;
and U4, the user enters an identification analysis system to analyze according to the product identification to obtain product data.
2. The method of claim 1, wherein the step of encoding the identifier of the medical device in U2 comprises the following steps:
(1) coding important attribute information related to the production process including raw material purchase, outside service supply, factory inspection, warehouse management, component production, process matching, process inspection, whole machine assembly, delivery inspection, finished product inventory, sales order, installation and debugging and maintenance service, and recording a coding system of internal specifications of an enterprise on a material supplier and a material production date;
(2) after the raw material is processed, recording a minimum processing unit, a corresponding batch and a processing machine, simultaneously recording the information of workers who operate, and uniformly identifying codes in the processing procedure;
(3) performing quality detection and sample inspection on the processed product, marking the product after the quality detection is qualified, and accurately encoding the product to product specification, batch and single product according to the supervision requirement of the national drug administration on medical instruments;
(4) the enterprise uploads the coded product to a second-level node for medical instrument identifier analysis, the second-level node reports the product to a national drug administration for registration and filing, after the product passes the audit, the second-level node reports the product to a national top-level node for audit, after the product passes the top-level audit, the product is filed and stored, identifier registration is completed, and the identifier takes effect formally.
3. The identification coding method for medical instruments according to claim 2, wherein the specific steps of compatibility and unification of the U3 heterogeneous coding are as follows:
(1) before accessing the secondary node, the material coding and the product coding of an enterprise in production are carried out according to a private coding mode inside the enterprise, and meanwhile, after the enterprise accesses the secondary node, the enterprise assigns codes inside the enterprise by adopting a coding system of a secondary node identification analysis system;
(2) before accessing a secondary node, an enterprise needs to register an enterprise identification prefix in the secondary node, wherein the enterprise identification prefix is used as a unique ID of the enterprise in an industrial internet identification analysis system;
(3) the enterprise registers the coded product information in a second-level node, the second-level node reports the product information reported by the enterprise to the national drug administration for registration and filing, the product information is returned to the second-level node after the approval of the national drug administration, the second-level node reports the information to a national top-level node, the product information is registered after the top-level node passes, and the product information is stored by the second-level node by feeding back the result to the second-level node;
(4) when the enterprise uploads product information to the secondary node. The secondary node performs uniqueness assignment on the self-defined code of the product enterprise according to a code system, and codes the product in a mode of unique identification prefix and product identification suffix, so that the unique identification code of the product is completed;
(5) by means of the method of identifying the prefix and the product suffix, the unification of heterogeneous codes among enterprises is completed.
4. The method according to claim 3, wherein in step U4, the enterprise user of the identifier resolution system can use a self-built identifier resolution server or a secondary node identifier resolution hosting manner to resolve the product information, the self-built identifier resolution server needs to upload the IP address and port number corresponding to the identifier resolution server and an interface of identifier resolution when performing identifier registration and reporting information, and the secondary node requests to forward to a designated interface when receiving the identifier resolution. By using a secondary node hosting mode, detailed information of the identifier needs to be uploaded to a secondary node for identifier information registration, so that the secondary node completes identifier analysis work when receiving an analysis request.
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| CN113570383A (en) * | 2021-07-16 | 2021-10-29 | 湖北三赢兴光电科技股份有限公司 | Camera module batch number generation method, storage medium and chip |
| CN113780872A (en) * | 2021-09-22 | 2021-12-10 | 中国联合网络通信集团有限公司 | Product quality evaluation method, system and computer readable storage medium |
| CN113806406A (en) * | 2021-09-18 | 2021-12-17 | 王剑 | Diagnosis and treatment data storage method, query method and related device |
| CN113836868A (en) * | 2021-09-24 | 2021-12-24 | 中国联合网络通信集团有限公司 | Device encoding method, device identification platform, electronic device, and storage medium |
| CN113852921A (en) * | 2021-09-24 | 2021-12-28 | 中国联合网络通信集团有限公司 | Data transmission method, identification analysis platform, electronic device and storage medium |
| CN113923266A (en) * | 2021-10-27 | 2022-01-11 | 上海海洋工程装备制造业创新中心有限公司 | Ocean engineering equipment identification analysis method and system |
| CN114202187A (en) * | 2021-12-06 | 2022-03-18 | 南方电网数字电网研究院有限公司 | Power equipment intelligent identification analysis coding method based on power industry |
| CN117316413A (en) * | 2023-11-22 | 2023-12-29 | 祺遽(天津)信息科技有限公司 | Medical instrument life cycle management system based on UDI coding four-code mapping |
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Application publication date: 20210326 |