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Rumex 5-044

by Rumex International Co.

Rumex 5-044 is an ocular hook/spatula/manipulator (FDA Class I; FDA product code HNQ, Hook, Ophthalmic) made by Rumex International Co., listed in FDA GUDID since 1 Jun 2020 (UDI-DI 00840159909010), 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

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00840159909010 UDI-DI Date1 Jun 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Rumex
Generic name
Ocular hook/spatula/manipulator, reusable
Model / Ref / Catalog
5-044
Primary DI / UDI-DI
00840159909010
FDA product code
HNQ
GMDN term
Ocular hook/spatula/manipulator, reusable
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ocular hook/spatula/manipulator, reusable

Similar devices in this category

Other devices filed under Ocular hook/spatula/manipulator, reusable.

Other devices from Rumex International Co.

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Properties

  • Sterilise before use
  • Premarket exempt
Other properties (13, all answered No)