Integra® 602232
by Integra Lifesciences (Ireland) Limited
Integra® 602232 is a Class II device made by Integra Lifesciences (Ireland) Limited, listed in FDA GUDID since 7 Sep 2016 (UDI-DI 10381780168447), 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 | Number10381780168447 | Date7 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 10381780168447
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Integra®
- Generic name
- General-purpose light source
- Model / Ref / Catalog
- 602232
- Primary DI / UDI-DI
- 10381780168447
- FDA product code
- FCW
- GMDN term
- General-purpose light source
- Device class
- Class II
- Regulation number
- 876.1500
- GUDID distribution status
- In Commercial Distribution
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