Halyard 39224
Halyard 39224 (ELL18100TG) is a Class II device made by Avanos Medical, Inc., listed in FDA GUDID since 15 Mar 2017 (UDI-DI 10680651392241), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10680651392241 | Date15 Mar 2017 | StatusListed |
Official records
- AccessGUDID record 10680651392241
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Halyard
- Generic name
- Peripheral nerve-block blunt needle
- Model / Ref / Catalog
- 39224, ELL18100TG
- Primary DI / UDI-DI
- 10680651392241
- FDA product code
- CAZ
- GMDN term
- Peripheral nerve-block blunt needle
- Device class
- Class II
- Regulation number
- 868.5140
- GUDID distribution status
- In Commercial Distribution
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