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Zimmer 60-7075-103

by Hygia Health Services, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10817357022435 UDI-DI Date16 Feb 2018ListedStatusListed 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  • Withdrawn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
Zimmer
Generic Name
Tourniquet cuff, reprocessed
Model / Reference
60-7075-103
Primary DI / UDI-DI
10817357022435
FDA Product Code
KCY
GMDN Term
Tourniquet cuff, reprocessed
Device Class
Class I
Regulation Number
878.5910
GUDID distribution status
Not in Commercial Distribution

Other devices from Hygia Health Services, Inc.

See all devices from Hygia Health Services, Inc. →

Properties

  • Sterile
  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No