Halyard BPLA73-02
by Avid Medical, Inc. GUDID
Listed (no authorization)
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10809160540534 | Date12 Oct 2026 | StatusIn distribution |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — GUDID listing Listed
Recalls
No FDA recalls on record, checked 23 Oct 2026.
Specification
- Trade Name
- Halyard
- Generic Name
- General surgical procedure kit, non-medicated, single-use
- Model / Ref / Catalog
- BPLA73-02
- Primary DI / UDI-DI
- 10809160540534
- FDA Product Code
- OHD
- GMDN Term
- General surgical procedure kit, non-medicated, single-use
- Device Class
- Class II
- Regulation Number
- 884.1720
- Commercial Distribution
- In Commercial Distribution
Other devices from Avid Medical, Inc.
Properties
Other properties (7)
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Manufacturing Date: No