Taiwan FDA registration edcbd2774e12717b36d24435ea10fd62
"AGRA" osmotic analyzer (unsterilized)
TW: "愛科來" 滲透壓分析儀 (未滅菌)
Taiwan·Risk Class 1·ARKRAY FACTORY, INC.·Registered Aug 31, 2016 – Aug 31, 2026ActiveRegistration details
- Analysis ID
- edcbd2774e12717b36d24435ea10fd62
- Customs Code
- DHA09401694808
Company information
- Manufacturer
- ARKRAY FACTORY, INC.
- Manufacturer Country
- Japan
- Authorized Representative
- MEDTRI CO., LTD.
Product details
- Intended Use
- It is limited to the first level identification scope of the permeameter (A.2730) for clinical use.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2730 Permeameter for clinical use
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Aug 31, 2016
- Expiry Date
- Aug 31, 2026
About this record
Access comprehensive regulatory information for "AGRA" osmotic 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 edcbd2774e12717b36d24435ea10fd62 and manufactured by ARKRAY FACTORY, INC.. The authorized representative in Taiwan is MEDTRI CO., LTD..
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