Identity
- Trade Name
- 96`Adult Anesthesia Expandable Circuit FDA UDI
- Generic Name
- Anaesthesia breathing circuit, single-use FDA UDI
- Device Name
- 96`Adult Anesthesia Expandable Circuit, Bi-Wye, GSE, GSL, (2) BV, Medium Mask, 2L/Lf Ba FDA UDI
- Model / Reference
- 8035 FDA UDI
- Description
- 96`Adult Anesthesia Expandable Circuit, Bi-Wye, GSE, GSL, (2) BV, Medium Mask, 2L/Lf Ba FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00709078002649 FDA UDI
- FDA Product Code
- CAI FDA UDIOFP FDA UDICAH FDA UDI
- GMDN Term
- Anaesthesia breathing circuit, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5240 FDA UDI868.5260 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Anaesthesia breathing circuit, single-useHeat/moisture exchanger/microbial medical gas filter
96`Adult Anesthesia Expandable 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 85396ba4-8d33-4ae9-98a8-38c5bde258e3 33 fields · synced Jun 1, 2026