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Anneau +1 M2

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 19325/1

by Moria S.A.

Identity

Trade Name
ANNEAU +1 M2 EUDAMED
MORIA FDA UDI
Generic Name
Microkeratome FDA UDI
Device Name
ANNEAU +1 M2 EUDAMED
Model / Reference
19325/1 EUDAMED
M2 SUCTION RING +1 FDA UDI

Identifiers

Catalog Number
19325/1 FDA UDI
Primary DI / UDI-DI
03700483608355 EUDAMEDFDA UDI
Basic UDI-DI
B-03700483608355 EUDAMED
FDA Product Code
HMY FDA UDI
EMDN Code
Z1212020599 MICROKERATOMY INSTRUMENTS - OTHER EUDAMED
GMDN Term
Microkeratome FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
886.4370 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Anneau +1 M2 by Moria S.A. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

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

Sources (2)

  • EUDAMED 8131ceab-233c-40a5-a8e0-93cb5fc130c0 61 fields · synced Jun 19, 2026
  • FDA UDI 64549a79-94ed-4cc1-a6f0-7a94957ea7b3 33 fields · synced May 30, 2026