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Kaushik

by Kaushik Orthopaedic Private Limited 1,000+ variants

Ref KBKCN-013-018

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-08905926023893 Basic UDI-DI 08905926023893UDI-DIDate31 Aug 2026RegisteredStatusActive

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  • Withdrawn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
traumaHeal Bend Kuntscher Cloverleaf Nail, 13mm x 180 mm, Stainless Steel
Model / Reference
KBKCN-013-018
Primary DI / UDI-DI
08905926023893
Basic UDI-DI
B-08905926023893
EMDN Code
P09120201 Intramedullary nails
Device Class
Class IIb
EU market of registration
Austria

Manufacturer details

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

Other devices from Kaushik Orthopaedic Private Limited

See all devices from Kaushik Orthopaedic Private Limited →

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