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Dental Root Elevators

by M.A. Arain and Brothers (Pvt) Ltd. 3 variants

Ref 01-002-00

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 Number++G127DentalRootElevRUM3 Basic UDI-DI *+G12701002000R*UDI-DIDate17 Aug 2023RegisteredStatusActive

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  • Withdrawn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
Dental Root Elevators
Model / Reference
01-002-00
Primary DI / UDI-DI
*+G12701002000R*
Basic UDI-DI
++G127DentalRootElevRUM3
EMDN Code
Q0199 Odontology devices - other
Device Class
Class I
EU market of registration
Denmark

Manufacturer details

EUDAMED SRN
PK-MF-000012289
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from M.A. Arain and Brothers (Pvt) Ltd.

Properties

  • Sterile
  • Reusable

Other properties (11)

  • 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