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Kendall 31479549

by Cardinal Health 200, LLC

Kendall 31479549 is a Class II device made by Cardinal Health 200, LLC, listed in FDA GUDID since 27 May 2022 (UDI-DI 10192253040500), 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 Number10192253040500 UDI-DI Date27 May 2022ListedStatusListed 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  • Withdrawn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
31479549
Primary DI / UDI-DI
10192253040500
FDA product code
HGP
GMDN term
Foetal scalp electrode, spiral
Device class
Class II
Regulation number
884.2675
GUDID distribution status
In Commercial Distribution

Related devices

Category: Foetal scalp electrode, spiral

Similar devices

Other devices filed under FDA product code HGP (Electrode, circular (spiral), scalp and applicator).

Other devices from Cardinal Health 200, LLC

See all devices from Cardinal Health 200, LLC →

Properties

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