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Bellast Prime (Mild)

EUDAMED

Class III (EU MDR)

Ref MPF10M

by GENOSS Co., Ltd.

Identity

Trade Name
Bellast Prime (Mild) EUDAMED
Device Name
Bellast Prime (Mild) EUDAMED
Model / Reference
MPF10M EUDAMED

Identifiers

Primary DI / UDI-DI
08800026543480 EUDAMED
Basic UDI-DI
B-08800026543480 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

Bellast Prime (Mild) 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 94d5fec4-fdeb-43e0-99ac-d0b432e8f713 61 fields · synced Sep 18, 2026