Rumex 12-321

by Rumex International Co.

Rumex 12-321 is a Class I device made by Rumex International Co., listed in FDA GUDID since 27 Jul 2020 (UDI-DI 00840159902523), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00840159902523 UDI-DI	Date27 Jul 2020Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00840159902523

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Rumex
Generic name: Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable
Model / Ref / Catalog: 12-321

Primary DI / UDI-DI: 00840159902523
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

Similar devices in this category

Other devices filed under Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable.

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Properties

Sterilise before use
Premarket exempt

Other properties (13, all answered No)