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Starfit Nasogastric Feeding and Aspiration Tube with Guidewire NGGV14-120

by Hoist Medical

Ref NGGV14-120Model STARFIT NASOGASTRIC FEEDING AND ASPIRATION TUBE WITH GUIDEWIRE

Active European Union

CE MDR

Valid until

31 Oct 2029

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier DQS Medizinprodukte GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 26 Oct 2026. What this means

Regulatory status

as of registry sync 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number1000217799 Date14 Feb 2025IssuedStatusActive expires 31 Oct 2029

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 1000217799 Active

    Quality management system EU MDR

    Certifier
    DQS Medizinprodukte GmbH 0297
    Issued
    14 Feb 2025
    Expires
    31 Oct 2029

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Starfit Nasogastric Feeding and Aspiration Tube with Guidewire
Model / Reference
STARFIT NASOGASTRIC FEEDING AND ASPIRATION TUBE WITH GUIDEWIRE, NGGV14-120
Primary DI / UDI-DI
03760348111536
Basic UDI-DI
376034811200.07BL
Direct Marketing DI
03760348111536
EMDN Code
G02020101 Nasogastric tubes
Device Class
Class IIa
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
FR-MF-000026140

Other devices from Hoist Medical

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Properties

  • Sterile
  • Administering Medicine

Other properties (11)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No