Taiwan FDA registration 0f51ffd0f42c90fb745fe4fb3c948fc4
"Helena" QuickGel Serum Protein kit (Non-Sterile)
TW: "賀蓮那" 血清蛋白試劑 (未滅菌)
Taiwan·Risk Class 1·MD·HELENA LABORATORIES, INC.·Registered Aug 03, 2016 – Aug 03, 2021ExpiredRegistration details
- Analysis ID
- 0f51ffd0f42c90fb745fe4fb3c948fc4
- License Form
- Ministry of Health Medical Device Import No. 016858
- Customs Code
- DHA09401685807
Company information
- Manufacturer
- HELENA LABORATORIES, INC.
- Manufacturer Country
- Japan
- Authorized Representative
- SHANG LI INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the total protein test system (A.1635) of the Measures for the Administration of 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
Dates and status
- Registration Date
- Aug 03, 2016
- Expiry Date
- Aug 03, 2021
About this record
Access comprehensive regulatory information for "Helena" QuickGel Serum Protein kit (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 0f51ffd0f42c90fb745fe4fb3c948fc4 and manufactured by HELENA LABORATORIES, INC.. The authorized representative in Taiwan is SHANG LI INSTRUMENTS CO., LTD..
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