Skip to content

Kendall 31479846

by Cardinal Health 200, LLC

Ref 31479846Model KENDALL Fetal Spiral Electrode Cable

Kendall 31479846 is a device classified as Class I in the EU and Class II in the US made by Cardinal Health 200, LLC, registered in EUDAMED on 17 Sep 2026 (Basic UDI-DI 0630140000000000000010869) and listed in FDA GUDID since 16 Jul 2021 (UDI-DI 10885380181047), active as of 23 Oct 2026.

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

CE MDR

Valid until

No date given

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

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0630140000000000000010869 Basic UDI-DI 10885380181047UDI-DIDate17 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10885380181047 UDI-DI Date16 Jul 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0630140000000000000010869 registered 17 Sep 2026 Active
  • FDA GUDID UDI-DI 10885380181047 listed 16 Jul 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10885380181047
  2. Registered EUDAMED 0630140000000000000010869

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  • Withdrawn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
Kendall
Generic name
Electrical-only medical device connection cable, reusable
Device name
KENDALL Fetal Spiral Electrode Cable
Model / Ref / Catalog
31479846, KENDALL Fetal Spiral Electrode Cable
Primary DI / UDI-DI
10885380181047
Basic UDI-DI
0630140000000000000010869
FDA product code
IKD
EMDN code
Z12050380 Electrocardiographs - hardware accessories
GMDN term
Electrical-only medical device connection cable, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
890.1175
EU registration type
Standard device
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe
Size
Length — 2.25 Feet

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Electrical-only medical device connection cable, reusable

Similar devices in this category

Other devices filed under ELECTROCARDIOGRAPHS - HARDWARE ACCESSORIES.

Other devices from Cardinal Health 200, LLC

See all devices from Cardinal Health 200, LLC →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (21, all answered No)