Taiwan FDA registration 18a51cd5289b5090e9047c7105ebb7e9
"Arkra" aspartate transamine test strip per test
TW: "愛科來"天門冬胺酸轉胺每檢測試紙
Taiwan·Risk Class 2·ARKRAY Factory, Inc., Head office factory·Registered Dec 20, 2005 – Dec 20, 2025ExpiredRegistration details
- Analysis ID
- 18a51cd5289b5090e9047c7105ebb7e9
- Customs Code
- DHA00601569806
Company information
- Manufacturer
- ARKRAY Factory, Inc., Head office factory
- Manufacturer Country
- Japan
- Authorized Representative
- SYNGEN BIOTECH CO., LTD.
Product details
- Intended Use
- SPOTCHEM II GT trial is a test-tube diagnostic test drug that uses serum or plasma for quantitative determination of GET. This product is dedicated to SPOTCHEM instruments.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1100 天門冬胺酸轉胺酶試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Dec 20, 2005
- Expiry Date
- Dec 20, 2025
About this record
Access comprehensive regulatory information for "Arkra" aspartate transamine test strip per test in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 18a51cd5289b5090e9047c7105ebb7e9 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