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Cutegel

EUDAMED

Class III (EU MDR)

Ref CUModel ULTRARef CMModel MAXRef CAModel AQUA

by BNC KOREA, Inc.

Identity

Trade Name
CUTEGEL EUDAMED
Device Name
Cross-linked Hyaluronate Acid Dermal Filler EUDAMED
Model / Reference
ULTRA EUDAMED
CU EUDAMED
MAX EUDAMED
CM EUDAMED
AQUA EUDAMED
CA EUDAMED

Identifiers

Primary DI / UDI-DI
08809369092495 EUDAMED
08809369092488 EUDAMED
08809369092501 EUDAMED
Basic UDI-DI
B-08809369092495 EUDAMED
B-08809369092488 EUDAMED
B-08809369092501 EUDAMED
EMDN Code
P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany 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

Cutegel by BNC KOREA, Inc. — 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
BNC KOREA, Inc.
EUDAMED SRN
KR-MF-000008321
Authorised Representative
JaviTech e.K. DE-AR-000005875

Sources (3)

  • EUDAMED e2ededbc-b8e0-4cbf-95d3-42be07a3ed08 61 fields · synced Jul 28, 2026
  • EUDAMED 6471eace-0682-4383-ab14-12492ad32b9e 61 fields · synced May 17, 2026
  • EUDAMED 4f7a6d99-5557-487f-92c9-bd63974e3fec 61 fields · synced May 17, 2026