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Vivabella

EUDAMED

Class III (EU MDR)

Ref VA1081Model Vivabella50Ref VA1080Model Vivabella200

by VAIM Co., Ltd.

Identity

Trade Name
Vivabella EUDAMED
Device Name
Soft Tissue Injectable Implant EUDAMED
Model / Reference
Vivabella50 EUDAMED
VA1081 EUDAMED
Vivabella200 EUDAMED
VA1080 EUDAMED

Identifiers

Primary DI / UDI-DI
08800051300164 EUDAMED
08800051300140 EUDAMED
Basic UDI-DI
B-08800051300164 EUDAMED
B-08800051300140 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

Vivabella 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 (2)

  • EUDAMED b35cb59a-26bd-4e42-b2d0-8c8f187daa4c 61 fields · synced Jul 28, 2026
  • EUDAMED 24aee85a-9ca1-4344-b5b5-923be1561590 61 fields · synced May 17, 2026