Skip to content

Salem Sump 266122

by Cardinal Health 200, LLC

Ref 266122Model SALEM SUMP Dual Lumen Stomach Tube with Anti-Reflux Valve-2a

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number063014000000000000001856T Basic UDI-DI 10192253006872UDI-DIDate5 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10192253006872 UDI-DI Date16 Jan 2026ListedStatusListed GUDID: in commercial distribution

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

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Salem Sump
Generic Name
Nasogastric decompression tube
Device Name
SALEM SUMP Dual Lumen Stomach Tube with Anti-Reflux Valve-2a
Model / Ref / Catalog
266122, SALEM SUMP Dual Lumen Stomach Tube with Anti-Reflux Valve-2a
Primary DI / UDI-DI
10192253006872
Basic UDI-DI
063014000000000000001856T
FDA Product Code
FEG
EMDN Code
G02020101 Nasogastric tubes
GMDN Term
Nasogastric decompression tube
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
876.5980
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution
Size
Catheter Gauge — 14 French

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class II

Other devices from Cardinal Health 200, LLC

See all devices from Cardinal Health 200, LLC →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (18)

  • 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
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No