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Fg 21.010

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-07630958200493 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  • Withdrawn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 21.010
Fg Xl 21.010
Fg 21R.010
Fg 23.010
Fg 21L.010
Fg 21.012
Fg 21RX.010
Fg 21.014
Fg 21.016
Fg S 2.010
Fg 2.010
Device Name
Fg 21.010 Cyl. Square Fg 19 010
Fg Xl 21.010 Cyl. Square Fg 25 010
Fg 21R.010 Cyl. Round Fg 19 010
Fg 23.010 Cone Square Fg 19 010
Fg 21L.010 Cyl. Square Fg 21 010
Fg 21.012 Cyl. Square Fg 19 012
Fg 21RX.010 Dc Cyl. Round Fg 19 010
Fg 21.014 Cyl. Square Fg 19 014
Fg 21.016 Cyl. Square Fg 19 016
Fg S 2.010 Invert Cone Fg 16.5 010
Fg 2.010 Inverted Cone Fg 19 010
Model / Reference
Carbide bur, ROT V10.2024
Primary DI / UDI-DI
07630958200493, 07630958216838, 07630958200608, 07630958200653, 07630958200561, 07630958200516, 07630958202343, 07630958200530, 07630958200554, 07630958200127, 07630958200356
Basic UDI-DI
B-07630958200493, B-07630958216838, B-07630958200608, B-07630958200653, B-07630958200561, B-07630958200516, B-07630958202343, B-07630958200530, B-07630958200554, B-07630958200127, B-07630958200356
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