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60-7600-003-00

by Zimmer Orthopaedic Surgical Products

60-7600-003-00 is a Class I device made by Zimmer Orthopaedic Surgical Products, listed in FDA GUDID since 3 Nov 2021 (UDI-DI 00889024377776), 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 Number00889024377776 UDI-DI Date3 Nov 2021ListedStatusListed 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  • Withdrawn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

Generic name
Tourniquet cuff, reusable
Model / Ref / Catalog
60-7600-003-00
Primary DI / UDI-DI
00889024377776
FDA product code
KCY
GMDN term
Tourniquet cuff, reusable
Device class
Class I
Regulation number
878.5910
GUDID distribution status
In Commercial Distribution
Size
Length — 18 Inch

Related devices

Category: Tourniquet cuff, reusable

Other devices from Zimmer Orthopaedic Surgical Products

See all devices from Zimmer Orthopaedic Surgical Products →

Properties

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