Integra® 3714476
by Integra LifeSciences Production Corporation
Integra® 3714476 is a Class I device made by Integra LifeSciences Production Corporation, listed in FDA GUDID since 17 Sep 2018 (UDI-DI 10381780080343), 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 | Number10381780080343 | Date17 Sep 2018 | StatusListed |
Official records
- AccessGUDID record 10381780080343
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Integra®
- Generic name
- Nasal speculum, reusable
- Model / Ref / Catalog
- 3714476
- Primary DI / UDI-DI
- 10381780080343
- FDA product code
- EPY
- GMDN term
- Nasal speculum, reusable
- Device class
- Class I
- Regulation number
- 878.1800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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