Taiwan FDA registration 544fd98367ed367654d5b4542b62c328
“Sakura Finetek” Immunohistochemistry Reagents (Non-Sterile)
TW: “薩古拉凡鐵”免疫病理組織化學試劑(未滅菌)
Taiwan·Risk Class 1·MD·SAKURA FINETEK USA, INC.·Registered Dec 09, 2020 – Dec 09, 2025ExpiredRegistration details
- Analysis ID
- 544fd98367ed367654d5b4542b62c328
- License Form
- Ministry of Health Medical Device Import No. 022163
- Customs Code
- DHA09402216300
Company information
- Manufacturer
- SAKURA FINETEK USA, INC.
- Manufacturer Country
- United States
- Authorized Representative
- EVERLIGHT BIOTECH(TAIWAN) CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of immunopathological histochemical reagents and kits (B.1860) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B1860 Immunopathological histochemical reagents and kits
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 09, 2020
- Expiry Date
- Dec 09, 2025
About this record
Access comprehensive regulatory information for “Sakura Finetek” Immunohistochemistry Reagents (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 544fd98367ed367654d5b4542b62c328 and manufactured by SAKURA FINETEK USA, INC.. The authorized representative in Taiwan is EVERLIGHT BIOTECH(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