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Kendall 40000032

by Cardinalhealth

Kendall 40000032 is a Class II device made by Cardinalhealth, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10884521081123), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10884521081123 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Kendall
Generic name
Foetal scalp electrode, spiral
Model / Ref / Catalog
40000032
Primary DI / UDI-DI
10884521081123
FDA product code
HGP
GMDN term
Foetal scalp electrode, spiral
Device class
Class II
Regulation number
884.2675
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HGP (ELECTRODE, CIRCULAR (SPIRAL), SCALP AND APPLICATOR).

Other devices from Cardinalhealth

See all devices from Cardinalhealth →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)