Taiwan FDA registration e25cf5c3ec1598e5b9c3755a04f5fc0a
"Sysmex" UF-Fluorocell SF (Non-Sterile)
TW: "希森美康" 尿液分析用染色液 (未滅菌)
Taiwan·Risk Class 1·MD·SYSMEX INTERNATIONAL REAGENTS CO., LTD., ONO FACTORY·Registered Apr 22, 2016 – Apr 22, 2026CancelledRegistration details
- Analysis ID
- e25cf5c3ec1598e5b9c3755a04f5fc0a
- License Form
- Ministry of Health Medical Device Import No. 016432
- Customs Code
- DHA09401643202
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- SYSMEX TAIWAN CO., LTD.
Product details
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B1850 Dyes and chemical solution dyes
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 22, 2016
- Expiry Date
- Apr 22, 2026
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "Sysmex" UF-Fluorocell SF (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e25cf5c3ec1598e5b9c3755a04f5fc0a and manufactured by SYSMEX INTERNATIONAL REAGENTS CO., LTD., ONO FACTORY. The authorized representative in Taiwan is SYSMEX TAIWAN 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