Taiwan FDA registration 43b88047ac22559671e5091834fae565
"Unilux" electrotherapy device
TW: “優力舒活”電療器
Taiwan·Risk Class 2·ASTEK TECHNOLOGY LTD.·Registered Jul 16, 2019 – Mar 08, 2027ActiveRegistration details
- Analysis ID
- 43b88047ac22559671e5091834fae565
Company information
- Manufacturer
- ASTEK TECHNOLOGY LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Jinli Health Technology Co., Ltd.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5850 5850.
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Jul 16, 2019
- Expiry Date
- Mar 08, 2027
About this record
Access comprehensive regulatory information for "Unilux" electrotherapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 43b88047ac22559671e5091834fae565 and manufactured by ASTEK TECHNOLOGY LTD.. The authorized representative in Taiwan is Jinli Health Technology Co., Ltd..
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