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Lenisna

EUDAMED

Class III (EU MDR)

Ref VA1052Model Lenisna200

by VAIM Co., Ltd.

Identity

Trade Name
Lenisna EUDAMED
Device Name
Soft Tissue Injectable Implant EUDAMED
Model / Reference
Lenisna200 EUDAMED
VA1052 EUDAMED

Identifiers

Primary DI / UDI-DI
08800051300003 EUDAMED
Basic UDI-DI
B-08800051300003 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 097428e3-899d-410c-903b-aee7daf46820 61 fields · synced Jun 18, 2026