Taiwan FDA registration 2f8144172023dfb4b1671ade6b15a3bd
"Helena" Capillary Serum Protein kit (Non-Sterile)
TW: "海倫那" 毛細管血清蛋白電泳套組(未滅菌)
Taiwan·Risk Class 1·MD·HELENA BIOSCIENCES EUROPE·Registered Apr 16, 2018 – Apr 16, 2023ExpiredRegistration details
- Analysis ID
- 2f8144172023dfb4b1671ade6b15a3bd
- License Form
- Ministry of Health Medical Device Import No. 018970
- Customs Code
- DHA09401897001
Company information
- Manufacturer
- HELENA BIOSCIENCES EUROPE
- Manufacturer Country
- United Kingdom
- Authorized Representative
- SHANG LI INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Protein (Chemical Separation Method) Test System (A.1630)".
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1630 Protein (Chemical Separation) Test System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 16, 2018
- Expiry Date
- Apr 16, 2023
About this record
Access comprehensive regulatory information for "Helena" Capillary 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 2f8144172023dfb4b1671ade6b15a3bd and manufactured by HELENA BIOSCIENCES EUROPE. The authorized representative in Taiwan is SHANG LI INSTRUMENTS CO., LTD..
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