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Wire Watch™ 021-1001

by Biotex, Inc.

Wire Watch 021-1001, a surgical drape clip (FDA Class I; FDA product code KGZ, Accessories, Catheter) made by Biotex, Inc., was listed in FDA GUDID on 9 Feb 2023 (UDI-DI M71002110010); the registry lists it as not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 NumberM71002110010 UDI-DI Date9 Feb 2023ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Wire Watch™
Generic name
Surgical drape clip, reusable
Model / reference
021-1001
Primary DI / UDI-DI
M71002110010
FDA product code
KGZ
GMDN term
Surgical drape clip, reusable
Device class
Class I
Regulation number
878.4200
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code KGZ (Accessories, Catheter).

Other devices from Biotex, Inc.

See all devices from Biotex, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)