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BiViDerma I

EUDAMED

Class III (EU MDR)

Ref BPLN-30Ref BPLN-30BCRef BPLN-30JC

by BioPlus Co., Ltd.

Identity

Trade Name
BiViDerma I EUDAMED
Device Name
BiViDerma I EUDAMED
Model / Reference
BPLN-30 EUDAMED
BPLN-30BC EUDAMED
BPLN-30JC EUDAMED

Identifiers

Primary DI / UDI-DI
08809639788721 EUDAMED
08809639782835 EUDAMED
08809639789056 EUDAMED
Basic UDI-DI
B-08809639788721 EUDAMED
B-08809639782835 EUDAMED
B-08809639789056 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

BiViDerma I 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 (3)

  • EUDAMED 15cb0041-f225-48c3-b29b-109728c509d0 61 fields · synced Jul 27, 2026
  • EUDAMED 6d5f3b51-100d-47e5-9935-8827cebbe25f 61 fields · synced May 17, 2026
  • EUDAMED 86ccccac-3ae6-4f62-b4ef-3c594650a9b6 61 fields · synced May 19, 2026