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Fg Q1.010

by Axis Dental SARL EUDAMED

Active European Union

Ref ROT V10.2024Model Carbide bur

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07630958202060 Basic UDI-DIDate12 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

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.

Specification

EUDAMED

Trade Name
Fg Q1.010
Fg Q1.018
Fg Q1.014
Fg Q1.016
Fg Q1.012
Device Name
Fg Q1.010 Excavabur Fg 19 010
Fg Q1.018 Excavabur Fg 19 018
Fg Q1.014 Excavabur Fg 19 014
Fg Q1.016 Excavabur Fg 19 016
Fg Q1.012 Excavabur Fg 19 012
Model / Reference
Carbide bur, ROT V10.2024
Primary DI / UDI-DI
07630958202060, 07630958202145, 07630958202107, 07630958202121, 07630958202084
Basic UDI-DI
B-07630958202060, B-07630958202145, B-07630958202107, B-07630958202121, B-07630958202084
EMDN Code
L159099 Odontostomatology instruments, reusable - other
Device Class
Class IIa
Market of Registration
France

Manufacturer details

EUDAMED SRN
CH-MF-000016224
Authorised representative
SL Medirep SAS FR-AR-000014715

Other devices from Axis Dental SARL

See all devices from Axis Dental SARL →

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