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MONALISA Lidocaine Filler

EUDAMED

Class III (EU MDR)

Ref MPF10SRef MPF10MRef MPF10H

by GENOSS Co., Ltd.

Identity

Trade Name
MONALISA Lidocaine Filler EUDAMED
Device Name
MONALISA Lidocaine Filler EUDAMED
Model / Reference
MPF10S EUDAMED
MPF10M EUDAMED
MPF10H EUDAMED

Identifiers

Primary DI / UDI-DI
08809552962871 EUDAMED
08809552962888 EUDAMED
08809552962895 EUDAMED
Basic UDI-DI
B-08809552962871 EUDAMED
B-08809552962888 EUDAMED
B-08809552962895 EUDAMED
EMDN Code
P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Northern Ireland 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

MONALISA Lidocaine Filler 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 (3)

  • EUDAMED fb49f476-4825-444f-a500-c8d1a45b7685 61 fields · synced Aug 3, 2026
  • EUDAMED 2b059331-41f1-4d4d-a2bf-6b04d11bc4d3 61 fields · synced May 17, 2026
  • EUDAMED b78562f6-3ce8-4ee6-879f-24cbc968e36f 61 fields · synced May 17, 2026