Taiwan FDA registration 120176f36eadc414a1cf82d83bb6797a
“PAJUNK” MultiStim Sensor/Switch
TW: “帕將克”神經刺激器
Taiwan·Risk Class 2·MD·PAJUNK GMBH MEDIZINTECHNOLOGIE·Registered May 20, 2019 – May 20, 2024ExpiredRegistration details
- Analysis ID
- 120176f36eadc414a1cf82d83bb6797a
- License Form
- Ministry of Health Medical Device Import No. 032611
- Customs Code
- DHA05603261100
Company information
- Manufacturer
- PAJUNK GMBH MEDIZINTECHNOLOGIE
- Manufacturer Country
- Germany
- Authorized Representative
- Huizhong Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D2775 Electronic peripheral nerve stimulator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 20, 2019
- Expiry Date
- May 20, 2024
About this record
Access comprehensive regulatory information for “PAJUNK” MultiStim Sensor/Switch in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 120176f36eadc414a1cf82d83bb6797a and manufactured by PAJUNK GMBH MEDIZINTECHNOLOGIE. The authorized representative in Taiwan is Huizhong Co., Ltd.
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