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Kaushik

by Kaushik Orthopaedic Private Limited 1,000+ variants

Ref KSP-T-SS-5.5-024Model 5.5mm

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08905926000160 Basic UDI-DI 08905926000160UDI-DIDate16 Sep 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  • Withdrawn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
Steffee Screw 5.5mm, Length 24mm, Titanium
Model / Reference
5.5mm, KSP-T-SS-5.5-024
Primary DI / UDI-DI
08905926000160
Basic UDI-DI
B-08905926000160
EMDN Code
P090799 Spinal prostheses and stabilisation systems - other
Device Class
Class IIb
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
IN-MF-000035697
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Kaushik Orthopaedic Private Limited

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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