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15 ml 33x20 Şurup Kadehi(ÇocukKi.Kap.)

by Senpa Plasti̇k Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇

Ref I0033

Active European Union

CE MDR

Valid until

15 Jan 2030

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SZUTEST Konformitätsbewertungsstelle GmbH

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 Number2975-MED-2501601 Date16 Jan 2025IssuedStatusActive expires 15 Jan 2030

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2975-MED-2501601 Active

    Quality assurance EU MDR

    Certifier
    SZUTEST Konformitätsbewertungsstelle GmbH 2975
    Issued
    16 Jan 2025
    Expires
    15 Jan 2030

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Şurup Kadehi/Syrup Cup
Model / Reference
I0033
Primary DI / UDI-DI
08682678537273
Basic UDI-DI
8682678537KDHNF
EMDN Code
V0399 Measurement devices - other
Device Class
Class I
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000034359

Other devices from Senpa Plasti̇k Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇

See all devices from Senpa Plasti̇k Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇ →

Properties

  • Measuring Function

Other properties (12)

  • 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
  • Incorporates Medicinal Product: No