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Diamatrix H380-.5-T

by Diamatrix

Diamatrix H380-.5-T is an ocular hook/spatula/manipulator (FDA Class I; FDA product code HNQ, Hook, Ophthalmic) made by Diamatrix, listed in FDA GUDID since 30 Oct 2019 (UDI-DI 00813059015105), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00813059015105 UDI-DI Date30 Oct 2019ListedStatusListed 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  • Withdrawn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
Diamatrix
Generic name
Ocular hook/spatula/manipulator, reusable
Model / reference
H380-.5-T
Primary DI / UDI-DI
00813059015105
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
Sterilisation method
Moist Heat or Steam Sterilization

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 Diamatrix

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)