Taiwan FDA registration 07301d200d79371cfa91a40a4b6a63f7
"Arkray" SPOTCHEM D TP Reagent Strip (Non-sterile)
TW: "愛科來" 總蛋白質檢測試紙(未滅菌)
Taiwan·Risk Class 1·MD·ARKRAY Factory, Inc., Head office factory·Registered Dec 14, 2022 – Dec 14, 2027ActiveRegistration details
- Analysis ID
- 07301d200d79371cfa91a40a4b6a63f7
- License Form
- Ministry of Health Medical Device Import No. 022981
- Customs Code
- DHA09402298105
Company information
- Manufacturer
- ARKRAY Factory, Inc., Head office factory
- Manufacturer Country
- Japan
- Authorized Representative
- SYNGEN BIOTECH CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the total protein test system (A.1635) of the classification and grading management method for medical devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1635 Total Protein Test System
- Import Information
- Imported from abroad; GMP
Dates and status
- Registration Date
- Dec 14, 2022
- Expiry Date
- Dec 14, 2027
About this record
Access comprehensive regulatory information for "Arkray" SPOTCHEM D TP Reagent Strip (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 07301d200d79371cfa91a40a4b6a63f7 and manufactured by ARKRAY Factory, Inc., Head office factory. The authorized representative in Taiwan is SYNGEN BIOTECH CO., LTD..
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