Skip to content

NA Endo Leak Tester Adapter

by Medivators Inc. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00724995244460 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  • Withdrawn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
Endo Leak Tester Adapter, ZUTR10005S
Primary DI / UDI-DI
00724995244460
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