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Goosey Forceps

EUDAMED

Class I (EU MDR)

Ref 19090Model 2183

by Moria S.A.

Identity

Trade Name
GOOSEY FORCEPS EUDAMED
Device Name
Forcep. curved. serrated jaws 1 mm EUDAMED
Model / Reference
2183 EUDAMED
19090 EUDAMED

Identifiers

Primary DI / UDI-DI
03700483630479 EUDAMED
Basic UDI-DI
37004836Forceps1C2 EUDAMED
Direct Marketing DI
03700483630479 EUDAMED
EMDN Code
L170299 OPHTHALMOLOGY FORCEPS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

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

Goosey Forceps by Moria S.A. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

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

Sources (1)

  • EUDAMED d413a379-5ee3-4d50-989d-9d06ab385754 61 fields · synced Jun 19, 2026