Taiwan FDA registration 07699765bc098726b7b8062a002eea25
"AGRA" inorganic phosphoric acid test paper (unsterilized)
TW: "愛科來" 無機磷酸檢測試紙(未滅菌)
Taiwan·Risk Class 1·ARKRAY Factory, Inc.,Head office factory·Registered Jan 11, 2023 – Jan 11, 2028ActiveRegistration details
- Analysis ID
- 07699765bc098726b7b8062a002eea25
- Customs Code
- DHA09402301003
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 classification and grading management method of medical equipment, phosphoric acid (inorganic) test system (A.1580) first level identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1580 Phosphoric acid (inorganic) test system
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jan 11, 2023
- Expiry Date
- Jan 11, 2028
About this record
Access comprehensive regulatory information for "AGRA" inorganic phosphoric acid test paper (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 07699765bc098726b7b8062a002eea25 and manufactured by ARKRAY Factory, Inc.,Head office factory. The authorized representative in Taiwan is SYNGEN BIOTECH CO., LTD..
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