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Siora

by Siora Surgicals Pvt. Ltd. 1,000+ variants

Ref Ti.017.090

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08907536039189 Basic UDI-DI 08907536039189UDI-DIDate5 Mar 2024RegisteredStatusActive

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  • Withdrawn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
8.0mm Proximal Bolt Cannulated - Titanium Length 90mm
Model / Reference
Ti.017.090
Primary DI / UDI-DI
08907536039189
Basic UDI-DI
B-08907536039189
EMDN Code
P09120201 Intramedullary nails
Device Class
Class IIb
EU market of registration
Denmark

Manufacturer details

EUDAMED SRN
IN-MF-000036226
Authorised representative
Europecert UG (haftungsbeschränkt) DE-AR-000004974

Related devices

Category: Arthrodesis intramedullary nail, non-distracting

Other devices from Siora Surgicals Pvt. Ltd.

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Properties

  • Implantable

Other properties (10)

  • Sterile: No
  • 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