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Cutegel Lidocaine

EUDAMED

Class III (EU MDR)

Ref LLM2Model CL-Max1400

by BNC KOREA, Inc.

Identity

Trade Name
Cutegel Lidocaine EUDAMED
Device Name
Cross-linked Hyaluronate Acid Dermal Filler with Lidocaine EUDAMED
Model / Reference
CL-Max1400 EUDAMED
LLM2 EUDAMED

Identifiers

Primary DI / UDI-DI
08809369092914 EUDAMED
Basic UDI-DI
B-08809369092914 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

Cutegel Lidocaine 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 (1)

  • EUDAMED 3311c30e-8218-4f76-bcf5-c309bfb0a599 61 fields · synced Jun 20, 2026