Taiwan FDA registration ead59c6ef8dadb176c0e5f7f386874ff

"Helena" Capillary Urine Protein kit (Non-sterile)

TW: "海倫那" 毛細管尿蛋白電泳套組(未滅菌)

Taiwan·Risk Class 1·MD·HELENA BIOSCIENCES EUROPE·Registered Apr 18, 2018 – Apr 18, 2023Expired

Registration details

Analysis ID: ead59c6ef8dadb176c0e5f7f386874ff
License Form: Ministry of Health Medical Device Import No. 018977
Customs Code: DHA09401897702

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 18, 2018
Expiry Date: Apr 18, 2023

About this record

Access comprehensive regulatory information for "Helena" Capillary Urine 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 ead59c6ef8dadb176c0e5f7f386874ff and manufactured by HELENA BIOSCIENCES EUROPE. The authorized representative in Taiwan is SHANG LI INSTRUMENTS CO., LTD..

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