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NA Calibration Adapter

by Medivators Inc. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00724995244439 UDI-DIDate10 Jun 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Generic Name
Invasive medical device leak tester, electrical
Model / Ref / Catalog
Calibration Adapter, ZUTR10005CA
Primary DI / UDI-DI
00724995244439
FDA Product Code
FCY
GMDN Term
Invasive medical device leak tester, electrical
Device Class
Class I
Regulation Number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Invasive medical device leak tester, electrical

Other devices from Medivators Inc.

See all devices from Medivators Inc. →

Properties

  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No