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Kaushik

by Kaushik Orthopaedic Private Limited 15 variants

Ref KACLI-000

Active European Union

CE MDR

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/MDR Number8905926KACLI-0008J Basic UDI-DI 08905926060539UDI-DIDate28 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
ACL Instrument Set
Model / Reference
KACLI-000
Primary DI / UDI-DI
08905926060539
Basic UDI-DI
8905926KACLI-0008J
Direct Marketing DI
08905926060539
EMDN Code
L0919 Orthopaedic and traumatological surgery instrument kits, reusable
Device Class
Class I
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

See all devices from Kaushik Orthopaedic Private Limited →

Properties

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No