Durabase Soft

by Reliance Dental Manufacturing 2 variants

Ref Durabase Soft 4oz PowderModel Durabase Soft

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, self-declared

Class I: no certifier involved

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-D9471507 Basic UDI-DI D9471507UDI-DI	Date4 May 2026Registered	StatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name: Durabase Soft 4oz Powder
Model / Reference: Durabase Soft, Durabase Soft 4oz Powder

Primary DI / UDI-DI: D9471507
Basic UDI-DI: B-D9471507
EMDN Code: Q01020199 Dental impression materials - other

Device Class: Class I
EU market of registration: Italy

Manufacturer details

EUDAMED SRN: US-MF-000041470
Authorised representative: Kentzler-Kaschner Dental GmbH DE-AR-000006367

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Properties

Other properties (11)

Sterile: No
Implantable: No
Reusable: 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