Identity
- Trade Name
- AirLife Anesthesia Breathing Circuit FDA UDI
- Generic Name
- Anaesthesia breathing circuit, single-use FDA UDI
- Device Name
- 120" Expandable, Par-Wye, HMEF and B/V Filter, 3L Latex-Free Breathing Bag, 10' M/M GSL, Yankaur, Suction Tubing, Electrodes FDA UDI
- Model / Reference
- B9800 FDA UDI
- Description
- 120" Expandable, Par-Wye, HMEF and B/V Filter, 3L Latex-Free Breathing Bag, 10' M/M GSL, Yankaur, Suction Tubing, Electrodes FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10889483614891 FDA UDI
- 510(k) Number
- K951047 FDA UDI
- FDA Product Code
- CAH FDA UDI
- GMDN Term
- Anaesthesia breathing circuit, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5260 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Anaesthesia breathing circuit, single-use
AirLife Anesthesia Breathing Circuit by SunMed — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K951047 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- SunMed
Sources (1)
- FDA UDI f318c4ac-d960-43a7-8180-13132f297766 34 fields · synced May 30, 2026