Integra® Miltex® 19-437
by Integra LifeSciences Production Corporation
Integra® Miltex® 19-437 is a Class I device made by Integra LifeSciences Production Corporation, listed in FDA GUDID since 21 Dec 2017 (UDI-DI 10381780420064), 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 | Number10381780420064 | Date21 Dec 2017 | StatusListed |
Official records
- AccessGUDID record 10381780420064
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Integra® Miltex®
- Generic name
- Surgical soft-tissue manipulation forceps, alligator, reusable
- Model / Ref / Catalog
- 19-437
- Primary DI / UDI-DI
- 10381780420064
- FDA product code
- KAE
- GMDN term
- Surgical soft-tissue manipulation forceps, alligator, reusable
- Device class
- Class I
- Regulation number
- 874.4420
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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