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Kendall ES20211

by Cardinalhealth

Kendall ES20211 is a Class II device made by Cardinalhealth, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 20884527004772), 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 Number20884527004772 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  • Withdrawn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
Electrocardiographic electrode, single-use
Model / Ref / Catalog
ES20211
Primary DI / UDI-DI
20884527004772
FDA product code
DRX
GMDN term
Electrocardiographic electrode, single-use
Device class
Class II
Regulation number
870.2360
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electrocardiographic electrode, single-use

Similar devices in this category

Other devices filed under Electrocardiographic electrode, single-use.

Other devices from Cardinalhealth

See all devices from Cardinalhealth →

Properties

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