Taiwan FDA registration 1dac0194df3567946a229e6206796c7f
“Initia” Renova Electromagnetic Linear Shockwave Therapy Device and Accessories
TW: “英力夏”銳諾法電磁式柱狀震波治療系統與配件
Taiwan·Risk Class 3·MD·Initia Ltd.·Registered Jun 03, 2017 – Jun 03, 2022ExpiredRegistration details
- Analysis ID
- 1dac0194df3567946a229e6206796c7f
- License Form
- Ministry of Health Medical Device Import No. 029882
- Customs Code
- DHA05602988205
Company information
- Manufacturer
- Initia Ltd.
- Manufacturer Country
- Israel
- Authorized Representative
- SHAWHAN BIOMEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H9999 Other
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 03, 2017
- Expiry Date
- Jun 03, 2022
About this record
Access comprehensive regulatory information for “Initia” Renova Electromagnetic Linear Shockwave Therapy Device and Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1dac0194df3567946a229e6206796c7f and manufactured by Initia Ltd.. The authorized representative in Taiwan is SHAWHAN BIOMEDICAL CO., LTD..
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