Taiwan FDA registration 60806c957f98ad85a72cc5437dd40fce
Wanshimac comprehensive diagnosis and treatment instrument
TW: 萬適美綜合診療儀
Taiwan·Risk Class 2·SHINE ALPHA ELECTRONIC CO., LTD.·Registered Jan 28, 2012 – Jan 28, 2027ActiveRegistration details
- Analysis ID
- 60806c957f98ad85a72cc5437dd40fce
Company information
- Manufacturer
- SHINE ALPHA ELECTRONIC CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SHINE ALPHA ELECTRONIC CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order. For details, such as the approved copy of the Chinese imitation order (the original approval of the 101.05.04 approved copy of the imitation order and the approved label will be recycled and invalidated)
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5320 非植入式電子排尿自制裝置
- Import Information
- Domestic
Dates and status
- Registration Date
- Jan 28, 2012
- Expiry Date
- Jan 28, 2027
About this record
Access comprehensive regulatory information for Wanshimac comprehensive diagnosis and treatment instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 60806c957f98ad85a72cc5437dd40fce and manufactured by SHINE ALPHA ELECTRONIC CO., LTD.. The authorized representative in Taiwan is SHINE ALPHA ELECTRONIC CO., LTD..
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