Taiwan FDA registration 01ce53ab1574cb802674fea9a76056a4
"Venice" antipyretic patch (unsterilized)
TW: "威尼斯" 退熱貼 (未滅菌)
Taiwan·Risk Class 1·VENICE LABORATORIES CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 01ce53ab1574cb802674fea9a76056a4
Company information
- Manufacturer
- VENICE LABORATORIES CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- VENICE LABORATORIES 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 "Venice" antipyretic patch (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 01ce53ab1574cb802674fea9a76056a4 and manufactured by VENICE LABORATORIES CO., LTD.. The authorized representative in Taiwan is VENICE LABORATORIES CO., LTD..
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