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Brifill (Soft)

EUDAMED

Class III (EU MDR)

Ref MPF10S

by GENOSS Co., Ltd.

Identity

Trade Name
Brifill (Soft) EUDAMED
Device Name
Brifill (Soft) EUDAMED
Model / Reference
MPF10S EUDAMED

Identifiers

Primary DI / UDI-DI
08800026543350 EUDAMED
Basic UDI-DI
B-08800026543350 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

Brifill (Soft) 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 f64da2a4-8630-4349-97d5-86e02b398c48 61 fields · synced Jul 18, 2026