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ReMedium Advance-H

EUDAMED

Class III (EU MDR)

Ref BPL100-60BC

by BioPlus Co., Ltd.

Identity

Trade Name
ReMedium Advance-H EUDAMED
Device Name
ReMedium Advance-H EUDAMED
Model / Reference
BPL100-60BC EUDAMED

Identifiers

Primary DI / UDI-DI
08809947981869 EUDAMED
Basic UDI-DI
B-08809947981869 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

ReMedium Advance-H by BioPlus 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
BioPlus Co., Ltd.
EUDAMED SRN
KR-MF-000008618
Authorised Representative
KTR Europe GmbH DE-AR-000005685

Sources (1)

  • EUDAMED 5e9b1ac5-08c1-465b-a47e-11fdc1dd958b 61 fields · synced Jun 19, 2026