← Back to catalogue

Rejunos B-H

EUDAMED

Class III (EU MDR)

Ref BPL100-60C

by BioPlus Co., Ltd.

Identity

Trade Name
REJUNOS B-H EUDAMED
Device Name
REJUNOS B-H EUDAMED
Model / Reference
BPL100-60C EUDAMED

Identifiers

Primary DI / UDI-DI
08809947984341 EUDAMED
Basic UDI-DI
B-08809947984341 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

Rejunos B-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

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 71fa32b9-9bd3-48fa-bc03-35c2fea9d62d 61 fields · synced Jun 19, 2026