MORIA Bonn forceps
by Moria SA
MORIA Bonn forceps (20202X1) is an ophthalmic soft-tissue manipulation forceps (FDA Class I; FDA product code HNR, Forceps, Ophthalmic) made by Moria SA, listed in FDA GUDID since 15 Dec 2023 (UDI-DI 03700483609420), 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 | Number03700483609420 | Date15 Dec 2023 | StatusListed |
Official records
- AccessGUDID record 03700483609420
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Moria
- Generic name
- Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable
- Model / Ref / Catalog
- Bonn forceps, 20202X1
- Primary DI / UDI-DI
- 03700483609420
- FDA product code
- HNR
- GMDN term
- Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable
- Device class
- Class I
- Regulation number
- 886.4350
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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