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Herafill Ultra Volume H

EUDAMED

Class III (EU MDR)

Ref BPL100-60BCRef BPL100-60C

by BioPlus Co., Ltd.

Identity

Trade Name
Herafill Ultra Volume H EUDAMED
Device Name
Herafill Ultra Volume H EUDAMED
Model / Reference
BPL100-60BC EUDAMED
BPL100-60C EUDAMED

Identifiers

Primary DI / UDI-DI
08809947983993 EUDAMED
08809947983986 EUDAMED
Basic UDI-DI
B-08809947983993 EUDAMED
B-08809947983986 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

Herafill Ultra Volume 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

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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 7e66c7d1-1c93-47eb-a124-24d2a688ba57 61 fields · synced Sep 30, 2026
  • EUDAMED 76b31bba-62aa-4eec-8d12-972b5fbf4359 61 fields · synced May 18, 2026