Forceps 35-449-07-07
Forceps 35-449-07-07 is a Class I device made by KLS-Martin L.P., listed in FDA GUDID since 26 Sep 2018 (UDI-DI 00888118056429), 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 | Number00888118056429 | Date26 Sep 2018 | StatusListed |
Official records
- AccessGUDID record 00888118056429
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Forceps
- Generic name
- Ophthalmic soft-tissue manipulation forceps, probe-like, reusable
- Model / reference
- 35-449-07-07
- Primary DI / UDI-DI
- 00888118056429
- FDA product code
- HNR
- GMDN term
- Ophthalmic soft-tissue manipulation forceps, probe-like, reusable
- Device class
- Class I
- Regulation number
- 886.4350
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices in this category
Other devices filed under Ophthalmic soft-tissue manipulation forceps, probe-like, reusable.
- Stephens Instruments ST5-7035 by KRISHNA IMPORTS INC
- Microforceps: Avci Foreign Body.(20 gauge / 0.9 mm) 2286.I by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
- Microforceps: End-gripping.(23 gauge / 0.6 mm) 1286.B06 by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
- 23g Ahmed Micro-Tying Forceps DFH-0003 by MicroSurgical Technology Inc.
- Stephens Instruments ST5-7000-25 by KRISHNA IMPORTS INC
- 23g Fine/Hoffman Capsulorhexis Forceps Head DFH-0002 by MicroSurgical Technology Inc.