Taiwan FDA registration 82c0b9b1702eb91904fc2beb4f7ae5d0
"Sato" Situnin antipyretic patch (unsterilized)
TW: “佐藤”適得寧退熱貼 (未滅菌)
Taiwan·Risk Class 1·DIA PHARMACEUTICAL CO., LTD. HYOGO FACTORY·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 82c0b9b1702eb91904fc2beb4f7ae5d0
- Customs Code
- DHA08401384309
Company information
- Manufacturer
- DIA PHARMACEUTICAL CO., LTD. HYOGO FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- SATO PHARMACEUTICAL 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
- import
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Sato" Situnin 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 82c0b9b1702eb91904fc2beb4f7ae5d0 and manufactured by DIA PHARMACEUTICAL CO., LTD. HYOGO FACTORY. The authorized representative in Taiwan is SATO PHARMACEUTICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices