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Biolife Skin Booster

EUDAMED

Class III (EU MDR)

Ref BPBN-31BCRef BPBN-31

by BioPlus Co., Ltd.

Identity

Trade Name
BIOLIFE SKIN BOOSTER EUDAMED
Device Name
BIOLIFE SKIN BOOSTER EUDAMED
Model / Reference
BPBN-31BC EUDAMED
BPBN-31 EUDAMED

Identifiers

Primary DI / UDI-DI
08809947984334 EUDAMED
08809947984327 EUDAMED
Basic UDI-DI
B-08809947984334 EUDAMED
B-08809947984327 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

Biolife Skin Booster 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 (2)

  • EUDAMED bb7d6c78-0ad9-4179-acc8-9eac7d9a5ced 61 fields · synced Aug 3, 2026
  • EUDAMED b9417521-4503-4fd1-96a8-f6b5e725cb99 61 fields · synced May 18, 2026