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Proback Towels WEPB800BL

by Crosstex International, Inc.

Proback Towels WEPB800BL is a Class I device made by Crosstex International, Inc., listed in FDA GUDID since 31 Oct 2022 (UDI-DI 50732224002823), 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 Number50732224002823 UDI-DI Date31 Oct 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  • Withdrawn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
Proback Towels
Generic name
Patient examination/treatment drape, single-use
Model / reference
WEPB800BL
Primary DI / UDI-DI
50732224002823
FDA product code
KHR
GMDN term
Patient examination/treatment drape, single-use
Device class
Class I
Regulation number
872.6050
GUDID distribution status
In Commercial Distribution

Related devices

Category: Patient examination/treatment drape, single-use

Similar devices

Other devices filed under FDA product code KHR (ABSORBER, SALIVA, PAPER).

Other devices from Crosstex International, Inc.

See all devices from Crosstex International, Inc. →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)