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Kendall 30951555

by Cardinalhealth

Kendall 30951555 is a Class I device made by Cardinalhealth, listed in FDA GUDID since 27 Jun 2018 (UDI-DI 20884527010391), 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 Number20884527010391 UDI-DI Date27 Jun 2018ListedStatusListed 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  • Withdrawn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
Abdominal binder, single-use
Model / Ref / Catalog
30951555
Primary DI / UDI-DI
20884527010391
FDA product code
FSD
GMDN term
Abdominal binder, single-use
Device class
Class I
Regulation number
880.5160
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FSD (BINDER, ABDOMINAL).

Other devices from Cardinalhealth

See all devices from Cardinalhealth →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)