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Vsorb

EUDAMED

Class III (EU MDR)

Ref DV2030T226CE

by PINE BM Co., Ltd.

Identity

Trade Name
VSORB EUDAMED
Device Name
DV2030T226CE EUDAMED
Model / Reference
DV2030T226CE EUDAMED

Identifiers

Primary DI / UDI-DI
08800058004416 EUDAMED
Basic UDI-DI
B-08800058004416 EUDAMED
EMDN Code
H010101010104 MOUNTED POLYDIOXANONE MONOFILAMENT WITH NEEDLE FOR TISSUE TRACTION (‘BARBED’) EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Czechia 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

Vsorb by PINE BM 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
PINE BM Co., Ltd.
EUDAMED SRN
KR-MF-000024222
Authorised Representative
Meta Biomed Europe GmbH DE-AR-000004953

Sources (1)

  • EUDAMED 146a35d2-d663-44af-9a44-bbea31a57b4f 61 fields · synced Jun 18, 2026