Identity
- Trade Name
- Valve, Bleed Tail FDA UDI
- Generic Name
- Mechanical expiratory valve, single-use FDA UDI
- Device Name
- Valve, Bleed Tail, Bulk(100/Cs) FDA UDI
- Model / Reference
- 7-00675 FDA UDI
- Description
- Valve, Bleed Tail, Bulk(100/Cs) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00709078010705 FDA UDI
- FDA Product Code
- CBP FDA UDI
- GMDN Term
- Mechanical expiratory valve, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5870 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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Mechanical expiratory valve, single-use
Valve, Bleed Tail by Westmed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- WaterPAP PRO Starter Kit — Airways Development, LLC · Class II
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
- Westmed, Inc.
Sources (1)
- FDA UDI b3798f7f-06cf-47e7-b601-ca0c7a974fa3 33 fields · synced May 29, 2026