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Diamond Flex 8/12mm

by Dentscare Ltda

Ref 4000002099

Diamond Flex 8/12mm (4000002099) is a Class I device made by Dentscare Ltda, registered in EUDAMED on 4 Nov 2026 (Basic UDI-DI 78996338PLS0016J), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number78996338PLS0016J Basic UDI-DI 07898032320202UDI-DIDate4 Nov 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Diamond Flex
Model / reference
4000002099
Primary DI / UDI-DI
07898032320202
Basic UDI-DI
78996338PLS0016J
EMDN code
Q01010403 Dental abrasive and polishing materials
Device class
Class I
EU registration type
Standard device
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
BR-MF-000004013
Authorised representative
Nuno Flores PT-AR-000003118

Similar devices in this category

Other devices filed under DENTAL ABRASIVE AND POLISHING MATERIALS.

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Properties

Other properties (14, all answered No)