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Honeyfill Hydro

EUDAMED

Class III (EU MDR)

Ref BPBN-31Ref BPBN-31BC

by BioPlus Co., Ltd.

Identity

Trade Name
HONEYFILL HYDRO EUDAMED
Device Name
HONEYFILL HYDRO EUDAMED
Model / Reference
BPBN-31 EUDAMED
BPBN-31BC EUDAMED

Identifiers

Primary DI / UDI-DI
08809947980022 EUDAMED
08809947980237 EUDAMED
Basic UDI-DI
B-08809947980022 EUDAMED
B-08809947980237 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

Honeyfill Hydro 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 e42f5723-d628-4205-be48-615704779191 61 fields · synced Jul 17, 2026
  • EUDAMED e2d1f7ea-d0d2-45f4-800d-39095f42f5fb 61 fields · synced May 19, 2026