Halyard 62160
by O&M Halyard Inc. GUDID
Withdrawn
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number20680651621607 | Date21 Apr 2016 | StatusWithdrawn |
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- Withdrawn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
- Sterilization packaging, single-use
- Model / Ref / Catalog
- 62160
- Primary DI / UDI-DI
- 20680651621607
- FDA Product Code
- FRG
- GMDN Term
- Sterilization packaging, single-use
- Device Class
- Class II
- Regulation Number
- 880.6850
- Commercial Distribution
- Not in Commercial Distribution
Other devices from O&M Halyard Inc.
Properties
Other properties (12)
- Sterile: No
- Implantable: No
- Contains Latex: No
- Prescription Use: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Expiration Date: No
- Manufacturing Date: No