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Unodent

by Falcon Surgical Co. (Pvt.) Ltd 450 variants

Ref IXW012

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, self-declared

Class I: no certifier involved

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/MDR Number++G120MDevicesNCalib9K Basic UDI-DI +G120IXW0120HUDI-DIDate9 May 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Medical Devices Non Calibrated
Model / Reference
IXW012
Primary DI / UDI-DI
+G120IXW0120H
Basic UDI-DI
++G120MDevicesNCalib9K
EMDN Code
V030201 Calipers
Device Class
Class I
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
PK-MF-000018125
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Falcon Surgical Co. (Pvt.) Ltd

See all devices from Falcon Surgical Co. (Pvt.) Ltd →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: 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