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Rumex 2-036T

by Rumex International Co.

Rumex 2-036T is a Class I device made by Rumex International Co., listed in FDA GUDID since 29 May 2020 (UDI-DI 00840159903933), 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 Number00840159903933 UDI-DI Date29 May 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  • Withdrawn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
Ophthalmic angular gauge, reusable
Model / Ref / Catalog
2-036T
Primary DI / UDI-DI
00840159903933
FDA product code
HLN
GMDN term
Ophthalmic angular gauge, reusable
Device class
Class I
Regulation number
886.1420
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ophthalmic angular gauge, reusable

Similar devices

Other devices filed under FDA product code HLN (Gauge, Lens, Ophthalmic).

Other devices from Rumex International Co.

See all devices from Rumex International Co. →

Properties

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