Na Microdeep Depth Electrode
by Dixi Medical France GUDID
Product code GZL
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number03664539000121 | Date14 Dec 2017 | StatusWithdrawn |
Coverage
- Listed
- Not covered
United States — GUDID listing Listed
Recalls
-
- Terminated Z-0535-2022
- Terminated Z-0542-2022
- Terminated Z-0541-2022
- Terminated Z-0540-2022
- Terminated Z-0538-2022
- Terminated Z-0537-2022
- Terminated Z-0536-2022
- Terminated Z-0534-2022
- Terminated Z-0539-2022
Potential deformation of the internal packaging (blister pack) could compromise sterile barrier of the device when removed from the Tyvek bag
Specification
- Trade Name
- Na
- Generic Name
- Depth electrode
- Model / Ref / Catalog
- MICRODEEP DEPTH ELECTRODE, D08-15CT
- Primary DI / UDI-DI
- 03664539000121
- 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
Other devices from Dixi Medical
Properties & raw data
Show properties, registry sources and raw records
Other properties (9)
- 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
- Manufacturing Date: No
Sources (1)
- FDA UDI 11173e8c-94ad-402c-9d1c-a1ce2116583a