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Nasogastric Catheter 10 Ch

by Türev İç Ve Diş Ti̇c. Anoni̇m Şi̇rketi̇ 2 variants

Ref 103 0601 1

Active European Union

CE MDR

Valid until

7 May 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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number2975-MED-2512801 Date8 May 2025IssuedStatusActive expires 7 May 2030

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2975-MED-2512801 Active

    Quality management system EU MDR

    Certifier
    SZUTEST Konformitätsbewertungsstelle GmbH 2975
    Issued
    8 May 2025
    Expires
    7 May 2030

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Nasogastric Catheter
Model / Reference
103 0601 1
Primary DI / UDI-DI
08682241350186
Basic UDI-DI
868224135TF04-NG-J7
Direct Marketing DI
08682241350186
EMDN Code
G020299 Gastrointestinal feeding/aspiration tubes - other
Device Class
Class IIa
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000039871

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Properties

  • Sterile

Other properties (12)

  • 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