Taiwan FDA registration 355bdcf6c05bbbad9e00144955b29f5b
Fide Hot and cold compress (unsterilized)
TW: 菲德 冷熱敷墊 (未滅菌)
Taiwan·Risk Class 1·TAIWAN STANCH CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 355bdcf6c05bbbad9e00144955b29f5b
Company information
- Manufacturer
- TAIWAN STANCH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TAIWAN STANCH CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, the first level identification range of "Medical Hot and Cold Compress Device (O.5700)".
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5700 醫療用冷熱敷裝置
- Import Information
- Domestic
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for Fide Hot and cold compress (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 355bdcf6c05bbbad9e00144955b29f5b and manufactured by TAIWAN STANCH CO., LTD.. The authorized representative in Taiwan is TAIWAN STANCH CO., LTD..
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