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MORIA Artificial chamber guide ring for ALTK

by Moria SA

MORIA Artificial chamber guide ring for ALTK (19164) is a corneal resection holder (FDA Class I; FDA product code HRH, Trephine, Manual, Ophthalmic) made by Moria SA, listed in FDA GUDID since 13 Dec 2023 (UDI-DI 03700483608140), 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 Number03700483608140 UDI-DI Date13 Dec 2023ListedStatusListed 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  • Withdrawn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
Moria
Generic name
Corneal resection holder, reusable
Model / Ref / Catalog
Artificial chamber guide ring for ALTK, 19164
Primary DI / UDI-DI
03700483608140
FDA product code
HRH
GMDN term
Corneal resection holder, 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: Corneal resection holder, reusable

Similar devices

Other devices filed under FDA product code HRH (Trephine, Manual, Ophthalmic).

Other devices from Moria SA

See all devices from Moria SA →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)