← Back to catalogue

Nimfia Volume

EUDAMED

Class III (EU MDR)

Ref BPLN2-60BC

by BioPlus Co., Ltd.

Identity

Trade Name
Nimfia Volume EUDAMED
Device Name
Nimfia Volume EUDAMED
Model / Reference
BPLN2-60BC EUDAMED

Identifiers

Primary DI / UDI-DI
08809947981180 EUDAMED
Basic UDI-DI
B-08809947981180 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

Nimfia Volume 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 0de08390-7a41-4ce3-9841-92b1b11b42f6 61 fields · synced Jun 19, 2026