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Denflex Spring Endo file

by Denflex Co., Ltd. EUDAMED 24 variants

Active European Union

Ref SFTG6HL25#10R-B

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08800181602343 Basic UDI-DIDate29 Dec 2022RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

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

Model / Reference
SFTG6HL25#10R-B
Primary DI / UDI-DI
08800181602343
Basic UDI-DI
B-08800181602343
EMDN Code
Q010199 Conservative dentistry and endodontics devices - other
Device Class
Class IIa
Market of Registration
Romania

Manufacturer details

EUDAMED SRN
KR-MF-000030617
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Denflex Co., Ltd.

See all devices from Denflex Co., Ltd. →

Properties

  • Reusable

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No