Skip to content

Apex

by Falcon Surgical Co. (Pvt.) Ltd 442 variants

Ref 2S01226

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++G120PPROBE3N Basic UDI-DI +G1202S012260FUDI-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  • Withdrawn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
Probes
Model / Reference
2S01226
Primary DI / UDI-DI
+G1202S012260F
Basic UDI-DI
++G120PPROBE3N
EMDN Code
L159003 Dental and periodontal probes and explorers, reusable
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