Rumex 16-0341T
Rumex 16-0341T is a Class I device made by Rumex International Co., listed in FDA GUDID since 22 Jun 2020 (UDI-DI 00840159903179), 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 | Number00840159903179 | Date22 Jun 2020 | StatusListed |
Official records
- AccessGUDID record 00840159903179
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Rumex
- Generic name
- Eyeball fixation instrument, reusable
- Model / Ref / Catalog
- 16-0341T
- Primary DI / UDI-DI
- 00840159903179
- FDA product code
- HNH
- GMDN term
- Eyeball fixation instrument, reusable
- Device class
- Class I
- Regulation number
- 886.4350
- GUDID distribution status
- In Commercial Distribution
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