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CoverGuard 101-101T

by Veridian Healthcare

CoverGuard 101-101T is a Class I device made by Veridian Healthcare, listed in FDA GUDID since 15 Aug 2025 (UDI-DI 00845717012294), registry data as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00845717012294 UDI-DI Date15 Aug 2025ListedStatusListed 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  • Withdrawn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
CoverGuard
Generic name
Skin-cover adhesive strip, non-antimicrobial
Model / reference
101-101T
Primary DI / UDI-DI
00845717012294
FDA product code
KGX
GMDN term
Skin-cover adhesive strip, non-antimicrobial
Device class
Class I
Regulation number
880.5240
GUDID distribution status
In Commercial Distribution

Related devices

Category: Skin-cover adhesive strip, non-antimicrobial

Similar devices in this category

Other devices filed under Skin-cover adhesive strip, non-antimicrobial.

Other devices from Veridian Healthcare

See all devices from Veridian Healthcare →

Properties

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