Taiwan FDA registration cf9d558a132f4c9164e7205556bef23e
"AGCO" Biochemistry Analyzer (Unsterilized)
TW: "愛科來" 生化分析儀 (未滅菌)
Taiwan·Risk Class 1·ARKRAY INDUSTRY, INC.·Registered Jan 11, 2022 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- cf9d558a132f4c9164e7205556bef23e
- Customs Code
- DHA084a0003901
Company information
- Manufacturer
- ARKRAY INDUSTRY, INC.
- Manufacturer Country
- Philippines
- Authorized Representative
- SYNGEN BIOTECH CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Individual Photometric Chemistry Analyzer for Clinical Use (A.2160)" of the Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2160 Individual Photometric Chemistry Analyzer for Clinical Use
Dates and status
- Registration Date
- Jan 11, 2022
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "AGCO" Biochemistry Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cf9d558a132f4c9164e7205556bef23e and manufactured by ARKRAY INDUSTRY, INC.. The authorized representative in Taiwan is SYNGEN BIOTECH 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