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Probe, 12cm

by Rhein Enterprises (Pvt) Ltd 3 variants

Ref RK-130-12R

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++G072RUPROBESDILATROS6Y Basic UDI-DI +G072RK13012R0IUDI-DIDate6 Feb 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Reusable, Stainless Steel, Non-Sterile Surgical Probes, Dilators and Sounds
Model / Reference
RK-130-12R
Primary DI / UDI-DI
+G072RK13012R0I
Basic UDI-DI
++G072RUPROBESDILATROS6Y
Direct Marketing DI
+G072RK13012R0I
EMDN Code
L0206 Grooved probes, reusable
Device Class
Class I
EU market of registration
Denmark

Manufacturer details

EUDAMED SRN
PK-MF-000036086
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Rhein Enterprises (Pvt) Ltd

See all devices from Rhein Enterprises (Pvt) Ltd →

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