Skip to content

Sinaspril Gel Voor Eerste Tandjes

by FARMACEUTICI PROCEMSA S.p.A Società Benefit

Ref 1131197

Active European Union

CE MDR

Valid until

25 Jun 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier KIWA CERMET ITALIA S.P.A.

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

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8002395procemsateeth1F2 Basic UDI-DI 08711744057602UDI-DIDate29 Jun 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MDR 00016-A Active

    Quality management system EU MDR

    Issued
    24 Jun 2026
    Expires
    25 Jun 2028

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Teething gel
Model / Reference
1131197
Primary DI / UDI-DI
08711744057602
Basic UDI-DI
8002395procemsateeth1F2
EMDN Code
Q0199 Odontology devices - other
Device Class
Class IIa
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
IT-MF-000047492

Other devices from FARMACEUTICI PROCEMSA S.p.A Società Benefit

See all devices from FARMACEUTICI PROCEMSA S.p.A Società Benefit →

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