← Back to catalogue

ReMedium Fine

EUDAMED

Class III (EU MDR)

Ref BPLN-30JC

by BioPlus Co., Ltd.

Identity

Trade Name
ReMedium Fine EUDAMED
Device Name
ReMedium Fine EUDAMED
Model / Reference
BPLN-30JC EUDAMED

Identifiers

Primary DI / UDI-DI
08809639789131 EUDAMED
Basic UDI-DI
B-08809639789131 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

ReMedium Fine 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
BioPlus Co., Ltd.
EUDAMED SRN
KR-MF-000008618
Authorised Representative
KTR Europe GmbH DE-AR-000005685

Sources (1)

  • EUDAMED ae4f1e56-7125-49a5-8f51-44e2edbd2a3a 61 fields · synced Jul 9, 2026