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Lenisna

EUDAMED

Class III (EU MDR)

Ref VA1011Model Lenisna50

by VAIM Co., Ltd.

Identity

Trade Name
Lenisna EUDAMED
Device Name
Soft Tissue Injectable Implant EUDAMED
Model / Reference
Lenisna50 EUDAMED
VA1011 EUDAMED

Identifiers

Primary DI / UDI-DI
08800051300041 EUDAMED
Basic UDI-DI
B-08800051300041 EUDAMED
EMDN Code
P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Türkiye 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

No

EUDAMED

Lenisna by VAIM 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
VAIM Co., Ltd.
EUDAMED SRN
KR-MF-000026357
Authorised Representative
JaviTech e.K. DE-AR-000005875

Sources (1)

  • EUDAMED 5afa262e-0df0-4b38-9c7d-1b1dc2596b3a 61 fields · synced Jul 30, 2026