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SALEM SUMP Gastroduodenal Tube-2a

by Cardinal Health 200 LLC 16 variants

Ref 1180264416Model SALEM SUMP Gastroduodenal Tube-2a

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0630140000000000000011668 Basic UDI-DI 10192253006957UDI-DIDate18 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
SALEM SUMP Gastroduodenal Tube-2a
Model / Reference
SALEM SUMP Gastroduodenal Tube-2a, 1180264416
Primary DI / UDI-DI
10192253006957
Basic UDI-DI
0630140000000000000011668
EMDN Code
G02020101 Nasogastric tubes
Device Class
Class IIa
EU market of registration
Ireland

Manufacturer details

EUDAMED SRN
US-MF-000006765
Authorised representative
Cardinal Health Ireland Manufacturing Limited IE-AR-000001988

Other devices from Cardinal Health 200, LLC

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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