Taiwan FDA registration 74d3221ddde0bf2c9d6c476a438df1b1
"Arkola" alkaline phosphatase test strip
TW: "愛科來"鹼性磷酸酶檢測試紙
Taiwan·Risk Class 2·ARKRAY Factory, Inc., Head office factory·Registered Jan 09, 2006 – Jan 09, 2026ExpiredRegistration details
- Analysis ID
- 74d3221ddde0bf2c9d6c476a438df1b1
- Customs Code
- DHA00601585601
Company information
- Manufacturer
- ARKRAY Factory, Inc., Head office factory
- Manufacturer Country
- Japan
- Authorized Representative
- SYNGEN BIOTECH CO., LTD.
Product details
- Intended Use
- Dedicated to SPOTCHEM instrument, in vitro diagnostic test drug for quantitative determination of ALP in serum or plasma.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1050 Alkaline phosphatase or isoenzyme testing system
- Import Information
- import
Dates and status
- Registration Date
- Jan 09, 2006
- Expiry Date
- Jan 09, 2026
About this record
Access comprehensive regulatory information for "Arkola" alkaline phosphatase test strip in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 74d3221ddde0bf2c9d6c476a438df1b1 and manufactured by ARKRAY Factory, Inc., Head office factory. 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