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Vsorb

by PINE BM Co., Ltd. 29 variants

Ref DV0045T227CE

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08800058004461 Basic UDI-DI 08800058004461UDI-DIDate5 Jun 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
DV0045T227CE
Model / Reference
DV0045T227CE
Primary DI / UDI-DI
08800058004461
Basic UDI-DI
B-08800058004461
EMDN Code
H010101010104 Mounted polydioxanone monofilament with needle for tissue traction (‘barbed’)
Device Class
Class III
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
KR-MF-000024222
Authorised representative
Meta Biomed Europe GmbH DE-AR-000004953

Other devices from PINE BM Co., Ltd.

See all devices from PINE BM Co., Ltd. →

Properties

  • Sterile
  • Implantable

Other properties (9)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No