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Anneau OU LC pour Chambre Artificielle

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 19186Model 17204

by Moria S.A.

Identity

Trade Name
Anneau OU LC pour Chambre Artificielle EUDAMED
ONE FDA UDI
Generic Name
Corneal resection holder, single-use FDA UDI
Device Name
ONE - ARTIFICIAL CHAMBER FOR SINGLE USE TREPHINE x1 EUDAMED
Model / Reference
17204 EUDAMED
19186 EUDAMED
OU LC GUIDE RING FOR ARTIFICIAL CHAMBER FDA UDI

Identifiers

Catalog Number
19186 FDA UDI
Primary DI / UDI-DI
03700483603428 EUDAMEDFDA UDI
Basic UDI-DI
37004836Art-chambers23P EUDAMED
FDA Product Code
HRH FDA UDI
EMDN Code
Q020299 CORNEA EXPLANTATION AND TRANSPLANTATION DEVICES - OTHER EUDAMED
GMDN Term
Corneal resection holder, single-use FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
886.4350 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Anneau OU LC pour Chambre Artificielle by Moria S.A. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Moria S.A.
EUDAMED SRN
FR-MF-000000336

Sources (2)

  • EUDAMED 44c5556b-2632-4f80-be9e-6562ba0b672e 61 fields · synced Jun 18, 2026
  • FDA UDI ed0c3da7-6056-4d34-a0ef-63b10c3caf2f 33 fields · synced May 30, 2026