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Moria Ou Lc 130 Head Artificial Chamber

by Moria SA

Moria Ou Lc 130 Head Artificial Chamber (19184/130) is a microkeratome (FDA Class I; FDA product code HNO, Keratome, Ac-Powered) made by Moria SA, listed in FDA GUDID since 7 May 2024 (UDI-DI 03700483603145), 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 Number03700483603145 UDI-DI Date7 May 2024ListedStatusListed 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  • Withdrawn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
Microkeratome
Model / Ref / Catalog
OU LC 130 HEAD ARTIFICIAL CHAMBER, 19184/130
Primary DI / UDI-DI
03700483603145
FDA product code
HNO
GMDN term
Microkeratome
Device class
Class I
Regulation number
886.4370
GUDID distribution status
In Commercial Distribution

Related devices

Category: Microkeratome

Similar devices

Also classified as Microkeratome.

Similar devices

Other devices filed under FDA product code HNO (Keratome, Ac-Powered).

Other devices from Moria SA

See all devices from Moria SA →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)