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CathGuard 7001-3920

by Reprocessing Products Corp

CathGuard 7001-3920 is a non-adhesive device retention bandage (FDA Class I; FDA product code KGX, Tape And Bandage, Adhesive) made by Reprocessing Products Corp, listed in FDA GUDID since 22 Aug 2019 (UDI-DI 00858293006182), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00858293006182 UDI-DI Date22 Aug 2019ListedStatusListed 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  • Withdrawn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
CathGuard
Generic name
Non-adhesive device retention bandage
Model / reference
7001-3920
Primary DI / UDI-DI
00858293006182
FDA product code
KGX
GMDN term
Non-adhesive device retention bandage
Device class
Class I
Regulation number
880.5240
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KGX (Tape And Bandage, Adhesive).

Other devices from Reprocessing Products Corp

See all devices from Reprocessing Products Corp →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)