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Na Connection Cable

by Dixi Medical France GUDID

Product code GZL

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number03664539001760 UDI-DIDate14 Dec 2017ListedStatusWithdrawn

Coverage

1 jurisdiction

United States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of America
  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls

9 recalls · FDA

  • 9 recalls, same reason

    • Terminated Z-0535-2022 FDA Class II initiated 9 Dec 2021
    • Terminated Z-0542-2022 FDA Class II initiated 9 Dec 2021
    • Terminated Z-0541-2022 FDA Class II initiated 9 Dec 2021
    • Terminated Z-0540-2022 FDA Class II initiated 9 Dec 2021
    • Terminated Z-0538-2022 FDA Class II initiated 9 Dec 2021
    • Terminated Z-0537-2022 FDA Class II initiated 9 Dec 2021
    • Terminated Z-0536-2022 FDA Class II initiated 9 Dec 2021
    • Terminated Z-0534-2022 FDA Class II initiated 9 Dec 2021
    • Terminated Z-0539-2022 FDA Class II initiated 9 Dec 2021

    Potential deformation of the internal packaging (blister pack) could compromise sterile barrier of the device when removed from the Tyvek bag

Specification

GUDID · synced 23 Oct 2026

Trade Name
Na
Generic Name
Depth electrode
Model / Ref / Catalog
CONNECTION CABLE, CBL-12/30
Primary DI / UDI-DI
03664539001760
510(k) Number
FDA Product Code
GZL
GMDN Term
Depth electrode
Device Class
Class II
Regulation Number
882.1330
Commercial Distribution
Not in Commercial Distribution
Size
Length — 30 Centimeter

Related devices

Cleared under the same submission (K170959)

Show all (12)

Other devices from Dixi Medical

See all devices from Dixi Medical →

Properties & raw data

Show properties, registry sources and raw records
  • Prescription Use
  • Serial Number
Other properties (12)
  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No

Sources (1)

  • FDA UDI 9921eef4-1583-47db-986f-c4d72d0cdb25 38 fields · synced 23 Oct 2026