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Volifil

EUDAMED

Class III (EU MDR)

Ref LL5P3Model Sub-Q

by BNC KOREA, Inc.

Identity

Trade Name
VOLIFIL EUDAMED
Device Name
Cross-linked Hyaluronate Acid Dermal Filler with Lidocaine EUDAMED
Model / Reference
Sub-Q EUDAMED
LL5P3 EUDAMED

Identifiers

Primary DI / UDI-DI
08809369093089 EUDAMED
Basic UDI-DI
B-08809369093089 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

Volifil 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 5ba4ae77-916d-4e57-a0ef-0eb9315e3011 61 fields · synced Jun 18, 2026