Skip to content

MORIA ONE - Punch D10.00mm x1

by Moria SA

MORIA ONE - Punch D10.00mm x1 (17200D1000) is a corneal punch set (FDA Class I; FDA product code HNJ, Punch, Corneo-Scleral) made by Moria SA, listed in FDA GUDID since 27 Dec 2023 (UDI-DI 03700483606160), 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 Number03700483606160 UDI-DI Date27 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  • Withdrawn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 punch set
Model / Ref / Catalog
ONE - Punch D10.00mm x1, 17200D1000
Primary DI / UDI-DI
03700483606160
FDA product code
HNJ
GMDN term
Corneal punch set
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution

Related devices

Category: Corneal punch set

Similar devices in this category

Other devices filed under Corneal punch set.

Other devices from Moria SA

See all devices from Moria SA →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)