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Strauss & Co - Industrial Diamonds Ltd

by Strauss & Co - Industrial Diamonds Ltd. 1,000+ variants

Ref D13F

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++D877strauss52 Basic UDI-DI D877D13F1UDI-DIDate7 May 2025RegisteredStatusActive

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

NorwayIcelandSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaLiechtensteinAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyTürkiyeCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

EU market availability

Made available in 32 countries, as listed in EUDAMED:

Declared by the manufacturer in EUDAMED for this device version; may not cover every market.

  • Austria since 15 Sep 2022
  • Belgium since 15 Sep 2022
  • Bulgaria since 15 Sep 2022
  • Croatia since 15 Sep 2022
  • Cyprus since 15 Sep 2022
  • Czechia since 15 Sep 2022
  • Denmark since 15 Sep 2022
  • Estonia since 15 Sep 2022
  • Finland since 15 Sep 2022
  • France since 15 Sep 2022
  • Germany since 15 Sep 2022
  • Greece since 15 Sep 2022
  • Hungary since 15 Sep 2022
  • Iceland since 15 Sep 2022
  • Ireland since 15 Sep 2022
  • Italy since 15 Sep 2022
  • Latvia since 15 Sep 2022
  • Liechtenstein since 15 Sep 2022
  • Lithuania since 15 Sep 2022
  • Luxembourg since 15 Sep 2022
  • Malta since 15 Sep 2022
  • Netherlands since 15 Sep 2022
  • Northern Ireland since 15 Sep 2022
  • Norway since 15 Sep 2022
  • Poland since 15 Sep 2022
  • Portugal since 15 Sep 2022
  • Romania since 15 Sep 2022
  • Slovakia since 15 Sep 2022
  • Slovenia since 15 Sep 2022
  • Spain since 15 Sep 2022
  • Sweden since 15 Sep 2022
  • Türkiye since 15 Sep 2022

Last checked 23 Oct 2026.

Specification

EUDAMED

Device Name
Diamond Dental Bur
Model / Reference
D13F
Primary DI / UDI-DI
D877D13F1
Basic UDI-DI
++D877strauss52
Unit of Use DI
1
EMDN Code
Q010199 Conservative dentistry and endodontics devices - other
Device Class
Class IIa
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
IL-MF-000019516
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

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Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: 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