Forceps 35-550-11-07
Forceps 35-550-11-07 is a Class I device made by KLS-Martin L.P., listed in FDA GUDID since 26 Sep 2018 (UDI-DI 00888118056443), 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 | Number00888118056443 | Date26 Sep 2018 | StatusListed |
Official records
- AccessGUDID record 00888118056443
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- Withdrawn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
- 35-550-11-07
- Primary DI / UDI-DI
- 00888118056443
- 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
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