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Drug Clinical alerts

by Synapse medicine

Ref Drug clinical alerts

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-DrugClinincalalertsCG Basic UDI-DI D-DrugClinincalalertsCGUDI-DIDate29 Jul 2023RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Drug Clinical alerts
Model / Reference
Drug clinical alerts
Primary DI / UDI-DI
D-DrugClinincalalertsCG
Basic UDI-DI
B-DrugClinincalalertsCG
EMDN Code
Z12040282 General medicine therapeutic treatment instruments - software accessories
Device Class
Class I
Special Device Type
-1192
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000009699

Other devices from Synapse medicine

See all devices from Synapse medicine →

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