DK2653183T3 - Nasale indgivelsesindretninger - Google Patents
Nasale indgivelsesindretninger Download PDFInfo
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- DK2653183T3 DK2653183T3 DK13177297.2T DK13177297T DK2653183T3 DK 2653183 T3 DK2653183 T3 DK 2653183T3 DK 13177297 T DK13177297 T DK 13177297T DK 2653183 T3 DK2653183 T3 DK 2653183T3
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M15/00—Inhalators
- A61M15/08—Inhaling devices inserted into the nose
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M11/00—Sprayers or atomisers specially adapted for therapeutic purposes
- A61M11/006—Sprayers or atomisers specially adapted for therapeutic purposes operated by applying mechanical pressure to the liquid to be sprayed or atomised
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M11/00—Sprayers or atomisers specially adapted for therapeutic purposes
- A61M11/006—Sprayers or atomisers specially adapted for therapeutic purposes operated by applying mechanical pressure to the liquid to be sprayed or atomised
- A61M11/007—Syringe-type or piston-type sprayers or atomisers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M11/00—Sprayers or atomisers specially adapted for therapeutic purposes
- A61M11/02—Sprayers or atomisers specially adapted for therapeutic purposes operated by air or other gas pressure applied to the liquid or other product to be sprayed or atomised
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M15/00—Inhalators
- A61M15/0001—Details of inhalators; Constructional features thereof
- A61M15/0003—Details of inhalators; Constructional features thereof with means for dispensing more than one drug
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M15/00—Inhalators
- A61M15/0001—Details of inhalators; Constructional features thereof
- A61M15/0013—Details of inhalators; Constructional features thereof with inhalation check valves
- A61M15/0015—Details of inhalators; Constructional features thereof with inhalation check valves located upstream of the dispenser, i.e. not traversed by the product
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M15/00—Inhalators
- A61M15/0001—Details of inhalators; Constructional features thereof
- A61M15/002—Details of inhalators; Constructional features thereof with air flow regulating means
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M15/00—Inhalators
- A61M15/0001—Details of inhalators; Constructional features thereof
- A61M15/0021—Mouthpieces therefor
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M15/00—Inhalators
- A61M15/009—Inhalators using medicine packages with incorporated spraying means, e.g. aerosol cans
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M15/00—Inhalators
- A61M15/0091—Inhalators mechanically breath-triggered
- A61M15/0098—Activated by exhalation
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M11/00—Sprayers or atomisers specially adapted for therapeutic purposes
- A61M11/06—Sprayers or atomisers specially adapted for therapeutic purposes of the injector type
- A61M11/08—Pocket atomisers of the injector type
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M15/00—Inhalators
- A61M15/0091—Inhalators mechanically breath-triggered
- A61M15/0095—Preventing manual activation in absence of inhalation
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M2202/00—Special media to be introduced, removed or treated
- A61M2202/04—Liquids
- A61M2202/0468—Liquids non-physiological
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M2202/00—Special media to be introduced, removed or treated
- A61M2202/06—Solids
- A61M2202/064—Powder
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M2205/00—General characteristics of the apparatus
- A61M2205/82—Internal energy supply devices
- A61M2205/8275—Mechanical
- A61M2205/8281—Mechanical spring operated
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- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Anesthesiology (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hematology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Mechanical Engineering (AREA)
- Otolaryngology (AREA)
- Pharmacology & Pharmacy (AREA)
- Infusion, Injection, And Reservoir Apparatuses (AREA)
- Medicinal Preparation (AREA)
- Medical Preparation Storing Or Oral Administration Devices (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Claims (23)
1. Nasal indgivelsesindretning til indgivelse af substans til en nasalluftvej hos et individ, omfattende: et mundstykke (119; 219; 319; 419; 519; 619; 919) igennem hvilket individet under brug udånder for at forårsage lukning af oropharyngeal velum af individet; et næsestykke (117; 217; 317; 417; 517; 617; 917) til tilpasning med et næsebor af et individ, næsestykket (117; 217; 317; 417; 517; 617; 917) inkluderer en dyse (149; 249; 349; 459; 549; 649; 949) igennem hvilken, under brug, substans indgives til nasalluftvejen; og et legemselement (121; 223; 321; 421; 521; 621; 921) som modtager en substansforsyningsenhed (120; 220; 320; 420; 520; 620; 920), hvor legemselementet (121; 223; 321; 421; 521; 621; 921) inkluderer et indløb (325; 525; 625; 925) som er i fluidforbindelse med mundstykket (119; 219; 319; 419; 519; 619; 919) og et udløb (327; 527; 627; 927) som er i fluidforbindelse med næsestykket (117; 217; 317; 417; 517; 617; 917); kendetegnet ved: en manuel-aktuerbar substansforsyningsenhed (120; 220; 320; 420; 520; 620; 920) til indgivelse af substans igennem dysen (149; 249; 349; 459; 549; 649; 949) af næsestykket (117; 217; 317; 417; 517; 617; 917), hvor substansforsyningsenheden (120; 220; 320; 420; 520; 620; 920) omfatter en legemedel (355; 655; 955) som er bevægelig fra en første hvileposition til en anden aktueret position ved manuel aktuering af substansforsyningsenheden (120; 220; 320; 420; 520; 620; 920), og indløbet (325; 525; 625; 925) af legemselementet (121; 223; 321; 421; 521; 621; 921) åbnes når legemedelen (355; 655; 955) af substansforsyningsenheden (120; 220; 320; 420; 520; 620; 920) bevæges til den aktuerede position, for derved at tilvejebringe en luftstrømning igennem næsestykket (117; 217; 317; 417; 517; 617; 917) samtidig med manuel aktuering af substansforsyningsenheden (120; 220; 320; 420; 520; 620; 920).
2. Indgivelsesindretning ifølge krav 1, endvidere omfattende: en rigelmekanisme (963) som kan betjenes mellem en første uvirksom konfiguration i hvilken substansforsyningsenheden (120; 220; 320; 420; 520; 620; 920) er uaktuerbar og en anden virksom konfiguration i hvilken substansforsyningsenheden (120; 220; 320; 420; 520; 620; 920) er aktuerbar.
3. Indgivelsesindretning ifølge krav 1 eller 2, hvor rigelmekanismen (963) er en åndedragsbetjent mekanisme som omfatter et rigelelement (967) som er bevægelig ved udånding af individet mellem en første uvirksom position i hvilken substansforsyningsenheden (120; 220; 320; 420; 520; 620; 920) er uaktuerbar og en anden virksom position i hvilken substansforsyningsenheden (120; 220; 320; 420; 520; 620; 920) er aktuerbar.
4. Indgivelsesindretning ifølge krav 3, hvor rigelmekanismen (963) omfatter et forspændingselement (969) til at forspænde rigelelementet (967) til den uvirksomme position.
5. Indgivelsesindretning ifølge krav 3 eller 4, hvor rigelmekanismen (963) omfatter et virksomt element som er koblet til rigelelementet (967) og betjent ved udåndingsvejrtrækning af individet til at bevæge rigelelementet (967) til den virksomme position.
6. Indgivelsesindretning ifølge krav 5, hvor det virksomme element omfatter et oppusteligt element som udvides ved udånding af individet.
7. Indgivelsesindretning ifølge et hvilket som helst af kravene 1 til 6, endvidere omfattende: en ventilanordning (125; 225; 425) som er i fluidforbindelse med mundstykket (119; 219; 319; 419; 519; 619; 919) og næsestykket (117; 217; 317; 417; 517; 617; 917), og kan betjenes mellem en lukket konfiguration i hvilken der ikke er fluidforbindelsesbane mellem mundstykket (119; 219; 319; 419; 519; 619; 919) og næsestykket (117; 217; 317; 417; 517; 617; 917) og en åben konfiguration ved aktuering af substansforsyningsenheden (120; 220; 320; 420; 520; 620; 920), således at for at forsyne en luftstrømning igennem næsestykket (117; 217; 317; 417; 517; 617; 917) ved aktuering af substansforsyningsenheden (120; 220; 320; 420; 520; 620; 920).
8. Indgivelsesindretning ifølge et hvilket som helst af kravene 1 til 6, endvidere omfattende: en strømkanal som fluidt forbinder næsestykket (117; 217; 317; 417; 517; 617; 917) og mundstykket (119; 219; 319; 419; 519; 619; 919), hvorved udåndet luft fra en udåndingsvejrtrækning indgives igennem næsestykket (117; 217; 317; 417; 517; 617; 917).
9. Indgivelsesindretning ifølge et hvilket som helst af kravene 1 til 8, hvor substansforsyningsenheden (120; 220; 320; 420; 520; 620; 920) er konfigureret til at blive manuelt nedtrykt af individet.
10. Indgivelsesindretning ifølge et hvilket som helst af kravene 1 til 8, endvidere omfattende: en påfyldningsmekanisme (221) som kan blive klargjort med en påfyldningskraft og manuelt aktueret til at påføre påfyldningskraften til substansforsyningsenheden (120; 220; 320; 420; 520; 620; 920), således for at aktuere den samme.
11. Indgivelsesindretning ifølge et hvilket som helst af kravene 1 til 10, hvor substansforsyningsenheden (120; 220; 320; 420; 520; 620; 920) omfatter et substans-indeholdende kammer (151; 251; 351; 461; 561; 651; 951) som tilvejebringer en volumen af substans til indgivelse af indgivelsesindretningen.
12. Indgivelsesindretning ifølge krav 11, hvor substansforsyningsenheden (120; 220; 320; 420; 520; 620; 920) endvidere omfatter et stempelelement (473; 573) som er bevægeligt i forhold til det substans-indeholdende kammer (151; 251; 351; 461; 561; 651; 951) til at indgive en dosis af substans fra det substansindeholdende kammer (151; 251; 351; 461; 561; 651; 951).
13. Indgivelsesindretning ifølge krav 12, hvor stempelelementet (473; 573) er bevægeligt mellem en flerhed af respektive positioner, således for at indgive en afmålt dosis af substans med hvert fremryk af stempelelementet (473; 573) mellem de respektive positioner.
14. Indgivelsesindretning ifølge krav 12 eller 13, hvor stempelelementet (473; 573) er bevægeligt i forhold til et legemselement (121; 223; 321; 421; 521; 621; 921) og et af stempelelementet (473; 573) og legemselementet (121; 223; 321; 421; 521; 621; 921) inkluderer et spor (577) som inkluderer sporafsnit (581a, 581b) som definerer hver af de respektive positioner, og den anden af stempelelementet (473; 573) og legemselementet (121; 223; 321; 421; 521; 621; 921) inkluderer en medfølger (531) som er placeret i sporet (577) og bevæget efter hinanden til hver af de respektive positioner ved aktuering af stempelelementet (473; 573).
15. Indgivelsesindretning ifølge et hvilket som helst af kravene 12 til 14, hvor substansforsyningsenheden (120; 220; 320; 420; 520; 620; 920) er en dobbeltdosis pumpeenhed, hvor stempelelementet (473; 573) er bevægeligt til to separate positioner.
16. Indgivelsesindretning ifølge et hvilket som helst af kravene 11 til 15, hvor det substans-indeholdende kammer (151; 251; 351; 461; 561; 651; 951) omfatter første og andet kammer (1001, 1003) hvilke hvert separat indeholder en respektiv substanskomponent (SI, S2) og tilvejebringer til rekonstitution af substanskomponenterne (SI, S2) for at tilvejebringe rekonstitueret substans til indgivelse af indgivelsesindretningen.
17. Indgivelsesindretning ifølge krav 16, hvor det substans-indeholdende kammer (151; 251; 351; 461; 561; 651; 951) endvidere omfatter et skrøbeligt element (1005) som normalt adskiller det første og andet kammer (1001, 1003) og når bristet tilvejebringer til rekonstituering af substanskomponenterne (SI, S2) for at tilvejebringe en rekonstitueret substans til indgivelse af indgivelsesindretningen.
18. Indgivelsesindretning ifølge krav 17, hvor indgivelsesindretningen inkluderer et bristende element (1021) som er konfigureret til at briste det skrøbelige element (1005) ved tilpasning af det substans-indeholdende kammer (151; 251; 351; 461; 561; 651; 951) til et hus (115; 215; 315; 415; 515; 615; 915) af indgivelsesindretningen.
19. Indgivelsesindretning ifølge et hvilket som helst af kravene 1 til 18, hvor næsestykket (117; 217; 317; 417; 517; 617; 917) inkludereret tætningselement (143; 243; 343; 453; 543; 643; 943) som tilvejebringeren tæt tætningstilpasning med næseboret af individet.
20. Indgivelsesindretning ifølge et hvilket som helst af kravene 1 til 19, endvidere omfattende: en strømregulator (629) som er konfigureret, med aktueringsbevægelse af substansforsyningsenheden (120; 220; 320; 420; 520; 620; 920), til at regulere strømkarakteristikker, såsom strømhastighed, strømprofil og strømvarighed, afen udåndingsluftstrøm som indgivet igennem næsestykket (117; 217; 317; 417; 517; 617; 917).
21. Indgivelsesindretning ifølge krav 20, hvor strømregulatoren (629) inkluderer en åbning (631) i hvilken strækker sig en bevægelig del af substansforsyningsenheden (120; 220; 320; 420; 520; 620; 920), således at, med aktueringsbevægelse af substansforsyningsenheden (120; 220; 320; 420; 520; 620; 920), det effektive område afen strømkanal til næsestykket (117; 217; 317; 417; 517; 617; 917) haren forudbestemmelig profil over aktueringsbevægelsen af substansforsyningsenheden (120; 220; 320; 420; 520; 620; 920).
22. Indgivelsesindretning ifølge et hvilket som helst af kravene 1 til 21, hvor substansforsyningsenheden (120; 220; 320; 420; 520; 620; 920) tilvejebringer indgivelsen afen pulversubstans eller en væskesubstans.
23. Indgivelsesindretning ifølge krav 22, hvor substansen indgives som en spray eller en stråle.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0719299.0A GB0719299D0 (en) | 2007-10-03 | 2007-10-03 | Nasal delivery devices |
GB0806808A GB2459266A (en) | 2007-10-03 | 2008-04-15 | Nasal delivery devices |
EP08836154.8A EP2197525B1 (en) | 2007-10-03 | 2008-10-03 | Nasal delivery devices |
Publications (1)
Publication Number | Publication Date |
---|---|
DK2653183T3 true DK2653183T3 (da) | 2015-06-08 |
Family
ID=40042313
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DK13177297.2T DK2653183T3 (da) | 2007-10-03 | 2008-10-03 | Nasale indgivelsesindretninger |
Country Status (17)
Country | Link |
---|---|
US (5) | US9067034B2 (da) |
EP (2) | EP2653183B1 (da) |
JP (3) | JP5778422B2 (da) |
KR (1) | KR101547502B1 (da) |
CN (1) | CN101918061B (da) |
AU (1) | AU2008306635A1 (da) |
BR (1) | BRPI0817502A2 (da) |
CA (1) | CA2701409C (da) |
DK (1) | DK2653183T3 (da) |
ES (2) | ES2436496T3 (da) |
GB (3) | GB0719299D0 (da) |
HK (1) | HK1145467A1 (da) |
IL (1) | IL204787A0 (da) |
MX (2) | MX355727B (da) |
PL (1) | PL2653183T3 (da) |
RU (1) | RU2506096C2 (da) |
WO (1) | WO2009044172A1 (da) |
Families Citing this family (103)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0114272D0 (en) | 2001-06-12 | 2001-08-01 | Optinose As | Nasal delivery device |
ZA200306564B (en) | 2001-02-26 | 2004-10-15 | Optinose As | Nasal devices. |
GB0215270D0 (en) * | 2002-07-02 | 2002-08-14 | Optinose As | Nasal devices |
GB0311570D0 (en) | 2003-05-20 | 2003-06-25 | Optinose As | Delivery device and method |
US7588033B2 (en) | 2003-06-18 | 2009-09-15 | Breathe Technologies, Inc. | Methods, systems and devices for improving ventilation in a lung area |
GB0319119D0 (en) | 2003-08-14 | 2003-09-17 | Optinose As | Delivery devices |
US7406966B2 (en) | 2003-08-18 | 2008-08-05 | Menlo Lifesciences, Llc | Method and device for non-invasive ventilation with nasal interface |
GB0320171D0 (en) * | 2003-08-28 | 2003-10-01 | Optinose As | Delivery devices |
GB0420513D0 (en) | 2004-09-15 | 2004-10-20 | Optinose As | Powder delivery devices |
GB0503738D0 (en) | 2005-02-23 | 2005-03-30 | Optinose As | Powder delivery devices |
WO2007035804A2 (en) | 2005-09-20 | 2007-03-29 | Lutz Freitag | Systems, methods and apparatus for respiratory support of a patient |
EP3546000A1 (en) | 2006-01-19 | 2019-10-02 | Optinose AS | Nasal administration |
GB0604444D0 (en) | 2006-03-06 | 2006-04-12 | Optinose As | Nasal devices |
GB0605799D0 (en) | 2006-03-23 | 2006-05-03 | Optinose As | Nasal delivery devices |
EP2023987B1 (en) | 2006-05-18 | 2016-11-09 | Breathe Technologies, Inc. | Tracheotomy device |
GB2438834A (en) | 2006-06-08 | 2007-12-12 | Optinose As | Intranasal protein administration |
GB2440316A (en) | 2006-07-25 | 2008-01-30 | Optinose As | Nasal inhaler with scrubber |
WO2008019102A2 (en) | 2006-08-03 | 2008-02-14 | Breathe Technologies, Inc. | Methods and devices for minimally invasive respiratory support |
GB0623732D0 (en) | 2006-11-28 | 2007-01-10 | Optinose As | Powder delivery devices |
GB0623731D0 (en) | 2006-11-28 | 2007-01-10 | Optinose As | Delivery device |
GB0623728D0 (en) | 2006-11-28 | 2007-01-10 | Optinose As | Delivery devices |
GB2448183A (en) | 2007-04-05 | 2008-10-08 | Optinose As | Nasal powder delivery device |
GB2448193A (en) | 2007-04-05 | 2008-10-08 | Optinose As | Nasal delivery device |
WO2008144589A1 (en) | 2007-05-18 | 2008-11-27 | Breathe Technologies, Inc. | Methods and devices for sensing respiration and providing ventilation therapy |
US8567399B2 (en) | 2007-09-26 | 2013-10-29 | Breathe Technologies, Inc. | Methods and devices for providing inspiratory and expiratory flow relief during ventilation therapy |
JP5513392B2 (ja) | 2007-09-26 | 2014-06-04 | ブリーズ・テクノロジーズ・インコーポレーテッド | 睡眠時無呼吸を治療するための方法及び装置 |
GB0719299D0 (en) | 2007-10-03 | 2007-11-14 | Optinose As | Nasal delivery devices |
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