Taiwan FDA registration c16159ca163c8fda08da7970e8dc8f05
"Taikang" antipyretic patch (unsterilized)
TW: “泰康”退熱貼 (未滅菌)
Taiwan·Risk Class 1·TAC KASEI CO., LTD.·Registered Aug 24, 2009 – Aug 24, 2019CancelledRegistration details
- Analysis ID
- c16159ca163c8fda08da7970e8dc8f05
- Customs Code
- DHA04400798507
Company information
- Manufacturer
- TAC KASEI CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- Shengfeng International Limited
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Medical Cold Compress Pack (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
- import
Dates and status
- Registration Date
- Aug 24, 2009
- Expiry Date
- Aug 24, 2019
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Taikang" 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 c16159ca163c8fda08da7970e8dc8f05 and manufactured by TAC KASEI CO., LTD.. The authorized representative in Taiwan is Shengfeng International Limited.
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