Codman® 451020
by Integra LifeSciences Production Corporation 2 variants
Codman® 451020 (45-1020) is a Class I device made by Integra LifeSciences Production Corporation, listed in FDA GUDID since 28 Feb 2020 (UDI-DI 10381780514268), 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 | Number10381780514268 | Date28 Feb 2020 | StatusListed |
Official records
- AccessGUDID record 10381780514268
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Codman®
- Generic name
- Epidural needle, non-threaded
- Model / Ref / Catalog
- 451020, 45-1020
- Primary DI / UDI-DI
- 10381780514268
- FDA product code
- HAO
- GMDN term
- Epidural needle, non-threaded
- Device class
- Class I
- Regulation number
- 882.4535
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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