Taiwan FDA registration 1a15068e66c1485781b15b248944917b
"SEKISUI" Clinimate NEFA Reagent (Non-Sterile)
TW: "積水" 克林美特游離脂肪酸檢測試劑 (未滅菌)
Taiwan·Risk Class 1·MD·SEKISUI MEDICAL CO., LTD. TSUKUBA PLANT·Registered Mar 18, 2016 – Mar 18, 2026ExpiredRegistration details
- Analysis ID
- 1a15068e66c1485781b15b248944917b
- License Form
- Ministry of Health Medical Device Import No. 016278
- Customs Code
- DHA09401627802
Company information
- Manufacturer
- SEKISUI MEDICAL CO., LTD. TSUKUBA PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- KUO'S YUAN IN ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the fatty acid test system (A.1290) of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1290 fatty acid testing system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 18, 2016
- Expiry Date
- Mar 18, 2026
About this record
Access comprehensive regulatory information for "SEKISUI" Clinimate NEFA Reagent (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 1a15068e66c1485781b15b248944917b and manufactured by SEKISUI MEDICAL CO., LTD. TSUKUBA PLANT. The authorized representative in Taiwan is KUO'S YUAN IN ENTERPRISE CO., LTD..
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