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Bone Curettes Halle 210mm FIG.3 Flexible

by Daddy D Pro

Ref DP-786-14-428

Active European Union

CE MDD

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 22 Oct 2026. What this means

Overview

BONE CURETTES HALLE 210MM FIG.3 FLEXIBLE is a cutting-edge medical device designed for precision bone curettage, offering unparalleled accuracy and safety in surgical procedures.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-B961DP786144280 Basic UDI-DI B961DP786144280UDI-DIDate21 Nov 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Model / Reference
DP-786-14-428
Primary DI / UDI-DI
B961DP786144280
Basic UDI-DI
B-B961DP786144280
EMDN Code
Q010399 Surgical dental devices - other
Device Class
Class I
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
PK-MF-000035172
Authorised representative
ANTEX MEDI SOLUTION DE-AR-000008078

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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