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Elega

EUDAMED

Class III (EU MDR)

Ref C4AsModel E-AquaRef C4NModel E-1

by BNC KOREA, Inc.

Identity

Trade Name
ELEGA EUDAMED
Device Name
Cross-linked Hyaluronate Acid Dermal Filler EUDAMED
Model / Reference
E-Aqua EUDAMED
C4As EUDAMED
E-1 EUDAMED
C4N EUDAMED

Identifiers

Primary DI / UDI-DI
08809369092686 EUDAMED
08809369092662 EUDAMED
Basic UDI-DI
B-08809369092686 EUDAMED
B-08809369092662 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

Elega 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 (2)

  • EUDAMED 214e3fef-a6af-4625-acfe-cce2efca0b8e 61 fields · synced Jul 11, 2026
  • EUDAMED a41e81ed-466f-464a-8f5e-0b5d509a5492 61 fields · synced May 18, 2026