Dento-Etch

by Spident 2 variants

Ref DEVP5-5

Active European Union

CE MDD

Valid until

No date given

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDD	NumberB-08809911113999 Basic UDI-DI 08809911113999UDI-DI	Date14 May 2026Registered	StatusActive

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

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device name: FineEtch
Model / reference: DEVP5-5

Primary DI / UDI-DI: 08809911113999
Basic UDI-DI: B-08809911113999
EMDN code: Q01010402 Enamel-dentinal etching materials

Device class: Class IIa
EU registration type: Legacy device (under a directive)
EU market of registration: France

Manufacturer details

EUDAMED SRN: KR-MF-000008691
Authorised representative: AR Experts B.V. NL-AR-000023989

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Properties

Other properties (12)

Supplied sterile: No
Sterilise before use: No
Implantable: No
Reusable: No
Contains latex: No
Reprocessed single-use device: No
Incorporates a substance derived from human blood or plasma: No
Contains human tissues or cells: No
Contains animal tissues or cells: No
Administering medicine: No
Measuring function: No
Incorporates a medicinal substance: No