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FlexiDiamond

by Cosmedent, Inc. 8 variants

Ref 502245

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number++D779STRIP101LM Basic UDI-DI D7795022450UDI-DIDate21 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberD7795022450 UDI-DI Date10 Feb 2020ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
FlexiDiamond Strips Narrow Coarse
Generic Name
Dental abrasive disk, single-use
Device Name
FlexiDiamond
Model / Reference
502245
Primary DI / UDI-DI
D7795022450 EUDAMED
D7795022451 GUDID
Basic UDI-DI
++D779STRIP101LM
FDA Product Code
EHM
EMDN Code
Q01010403 Dental abrasive and polishing materials
GMDN Term
Dental abrasive disk, single-use
Device Class
Class I
Regulation Number
872.6010
EU market of registration
Spain
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
D7795022450
GUDID
D7795022451

Manufacturer details

EUDAMED SRN
US-MF-000045496
Authorised representative
SAS Exclusivas Dentales S.L. ES-AR-000045423

Other devices from Cosmedent, Inc.

See all devices from Cosmedent, Inc. →

Properties

  • Single Use
  • Prescription Use
  • Premarket Exempt

Other properties (21)

  • 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
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No