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REVOFIL Aquashine BR

EUDAMED

Class III (EU MDR)

Ref N/AModel REVOFIL Aquashine BR

by Caregen Co., Ltd.

Identity

Trade Name
REVOFIL Aquashine BR EUDAMED
Device Name
Soft Filler EUDAMED
Model / Reference
REVOFIL Aquashine BR EUDAMED
N/A EUDAMED

Identifiers

Primary DI / UDI-DI
08809171384382 EUDAMED
Basic UDI-DI
B-08809171384382 EUDAMED
EMDN Code
Y062703 AESTHETIC FILLERS, CALF AND THIGH EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Latvia 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

REVOFIL Aquashine BR by Caregen 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
Caregen Co., Ltd.
EUDAMED SRN
KR-MF-000009948
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED f94ecbb2-ff1d-4945-81df-0c4779e3d484 61 fields · synced Jul 16, 2026