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Cap

by DIXI Medical France EUDAMEDGUDID

Ref ACS-050S-5Model Cap

Product code GZLEMDN N01800199

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number3664539CAPEM Basic UDI-DIDate30 Oct 2024RegisteredStatusActive
United StatesGUDID listing GUDID Number03664539000701 UDI-DIDate14 Dec 2017ListedStatusIn distribution

Coverage

2 jurisdictions

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 AmericaSwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Certificates: none listed in EUDAMED

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

EUDAMED · GUDID · synced 22 Oct 2026

Trade Name
Cap EUDAMED
Na GUDID
Generic Name
Depth electrode
Model / Ref / Catalog
Cap, ACS-050S-5, CAP FOR ANCHOR BOLT
Primary DI / UDI-DI
03664539000701
Basic UDI-DI
3664539CAPEM
Unit of Use DI
03664539003320
510(k) Number
FDA Product Code
GZL
EMDN Code
N01800199 Encephalic and peripheral nervous system surgical instruments, single-use - other
GMDN Term
Depth electrode
Device Class
Class I EUDAMED
Class II GUDID
Regulation Number
882.1330
Market of Registration
France
Commercial Distribution
In Commercial Distribution
MRI Safety
MR Unsafe

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
Cap
ACS-050S-5
GUDID
CAP FOR ANCHOR BOLT
Device ClassEUDAMED
Class I
GUDID
Class II

Manufacturer details

EUDAMED SRN
FR-MF-000005237

Other devices from Dixi Medical

See all devices from Dixi Medical →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
Other properties (19)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No

Sources (2)

  • EUDAMED 82ac3a20-d435-439e-ae0c-f976f34b9931 61 fields · synced 22 Oct 2026
  • FDA UDI d3c09c4f-04f2-4365-8154-c1326f5b6f78 36 fields · synced 30 May 2026