Identity
- Trade Name
- Disposable Anesthesia Circuit FDA UDI
- Generic Name
- Anaesthesia breathing circuit, single-use FDA UDI
- Device Name
- Anesthesia Circuit, Adult, 200" Expandable GSE, Parallel Wye, 2L Not made with latex breathing bag, 9910 series large adult mask, (2) BV filter, 15' x 0.038" ID M/M GSL, 20' Suction Tubing, Yankauer Sterile FDA UDI
- Model / Reference
- 9636 FDA UDI
- Description
- Anesthesia Circuit, Adult, 200" Expandable GSE, Parallel Wye, 2L Not made with latex breathing bag, 9910 series large adult mask, (2) BV filter, 15' x 0.038" ID M/M GSL, 20' Suction Tubing, Yankauer Sterile FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00709078005596 FDA UDI
- FDA Product Code
- OFP FDA UDI
- GMDN Term
- Anaesthesia breathing circuit, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5240 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Anaesthesia breathing circuit, single-use
Disposable Anesthesia Circuit by Westmed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 I | Pending data |
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Manufacturer
- Manufacturer
- Westmed, Inc.
Sources (1)
- FDA UDI cad57d4f-8510-480f-a6df-0ac943377082 33 fields · synced Jun 8, 2026