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ActivaScrew™ Interference TCP

by Bioretec Ltd. 30 variants

Ref B-DI-1030

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-06438394011892 Basic UDI-DI 06438394011892UDI-DIDate3 Dec 2021RegisteredStatusActive

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  • Withdrawn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
ActivaScrew™ Interference TCP 10 x 30 mm
Model / Reference
B-DI-1030
Primary DI / UDI-DI
06438394011892
Basic UDI-DI
B-06438394011892
EMDN Code
P09120605 Interference screws
Device Class
Class III
EU market of registration
Finland

Manufacturer details

EUDAMED SRN
FI-MF-000001328

Related devices

Category: Tendon/ligament bone anchor, non-bioabsorbable

Other devices from Bioretec Ltd.

See all devices from Bioretec 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