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edel X (Hard)

EUDAMED

Class III (EU MDR)

Ref MPF10H

by GENOSS Co., Ltd.

Identity

Trade Name
edel X (Hard) EUDAMED
Device Name
edel X (Hard) EUDAMED
Model / Reference
MPF10H EUDAMED

Identifiers

Primary DI / UDI-DI
08800026543411 EUDAMED
Basic UDI-DI
B-08800026543411 EUDAMED
EMDN Code
P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

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

Yes

EUDAMED

edel X (Hard) by GENOSS CO., Ltd. — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
GENOSS Co., Ltd.
EUDAMED SRN
KR-MF-000029064
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 0db599cc-aaab-42a9-8b4e-644aa5b58294 61 fields · synced Jun 19, 2026