Taiwan FDA registration e1e56a4ab92c6ce23629518a6915eae5
"Mai Pusher" pulse therapy machine
TW: “麥司推手”脈衝理療機
Taiwan·Risk Class 2·Chengyou An Technology Co., Ltd·Registered Nov 20, 2017 – Sep 19, 2020CancelledRegistration details
- Analysis ID
- e1e56a4ab92c6ce23629518a6915eae5
Company information
- Manufacturer
- Chengyou An Technology Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Max International Inc
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.5890 Transcutaneous electrical nerve stimulator for pain relief
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Nov 20, 2017
- Expiry Date
- Sep 19, 2020
- Cancellation Date
- Jun 17, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入;;許可證已逾有效期
About this record
Access comprehensive regulatory information for "Mai Pusher" pulse therapy machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e1e56a4ab92c6ce23629518a6915eae5 and manufactured by Chengyou An Technology Co., Ltd. The authorized representative in Taiwan is Max International Inc.
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