Taiwan FDA registration a1503dc5891f122c131cc4973c5e6e71
Erics Low Frequency Therapy Device
TW: 愛瑞克絲低週波治療器
Taiwan·Risk Class 2·Kaishen Limited·Registered Mar 23, 2012 – Mar 23, 2027ActiveRegistration details
- Analysis ID
- a1503dc5891f122c131cc4973c5e6e71
- Customs Code
- DHY00500362205
Company information
- Manufacturer
- Kaishen Limited
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SUNYOTEC MEDICAL CO., LTD.
Product details
- Intended Use
- Relieves shoulder soreness and peripheral nerve paralysis.
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.5890 Transcutaneous electrical nerve stimulator for pain relief
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Mar 23, 2012
- Expiry Date
- Mar 23, 2027
About this record
Access comprehensive regulatory information for Erics Low Frequency Therapy Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a1503dc5891f122c131cc4973c5e6e71 and manufactured by Kaishen Limited. The authorized representative in Taiwan is SUNYOTEC MEDICAL CO., LTD..
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