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REVOFIL Aquashine

EUDAMED

Class III (EU MDR)

Ref N/AModel REVOFIL Aquashine

by Caregen Co., Ltd.

Identity

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

Identifiers

Primary DI / UDI-DI
08809171381336 EUDAMED
08809171384375 EUDAMED
Basic UDI-DI
B-08809171381336 EUDAMED
B-08809171384375 EUDAMED
EMDN Code
Y062703 AESTHETIC FILLERS, CALF AND THIGH EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Denmark EUDAMED
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 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 (2)

  • EUDAMED 01ccca71-e955-439c-9b72-cc395801b46c 61 fields · synced Jul 22, 2026
  • EUDAMED 3c949efa-7bae-4ef7-9a70-60bd8850d83c 61 fields · synced May 19, 2026