DSA3500

by Dental International

Ref DSA3500

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, self-declared

Class I: no certifier involved

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

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number87193275323DSA3500HR Basic UDI-DI	Date8 Aug 2022Registered	StatusActive

Certificates

0 certificates · EUDAMED

No notified-body 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Withdrawn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/MDR Active

Specification

EUDAMED

Model / Reference: DSA3500

Primary DI / UDI-DI: 08719327532294, 08719327532287
Basic UDI-DI: 87193275323DSA3500HR
Direct Marketing DI: 08719327532294
08719327532287
EMDN Code: V9099 Various devices not included in other classes - other

Device Class: Class I
Market of Registration: Netherlands

Manufacturer details

EUDAMED SRN: NL-MF-000010964

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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