Taiwan FDA registration 87bc884dcf0166bccfa2b2ba6d0bf3f8
“PMT” DEPTHALON Depth electrode system
TW: “匹恩梯”深度電極系統
Taiwan·Risk Class 2·MD·PMT CORPORATION·Registered Sep 13, 2018 – Sep 13, 2023ExpiredRegistration details
- Analysis ID
- 87bc884dcf0166bccfa2b2ba6d0bf3f8
- License Form
- Ministry of Health Medical Device Import No. 031624
- Customs Code
- DHA05603162401
Company information
- Manufacturer
- PMT CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- WELLONG INSTRUMENTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K1330 depth electrode
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 13, 2018
- Expiry Date
- Sep 13, 2023
About this record
Access comprehensive regulatory information for “PMT” DEPTHALON Depth electrode system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 87bc884dcf0166bccfa2b2ba6d0bf3f8 and manufactured by PMT CORPORATION. The authorized representative in Taiwan is WELLONG INSTRUMENTS CO., LTD..
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