Taiwan FDA registration 4e186052a6c75b5af9aacc38b806e28b

"Helena" CSF Protein reagent Kit (Non-sterile)

TW: "海倫娜" 腦脊髓液蛋白試劑 (未滅菌)

Taiwan·Risk Class 1·MD·HELENA BIOSCIENCES EUROPE·Registered May 05, 2017 – May 05, 2022Expired

Registration details

Analysis ID: 4e186052a6c75b5af9aacc38b806e28b
License Form: Ministry of Health Medical Device Import No. 017792
Customs Code: DHA09401779208

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: May 05, 2017
Expiry Date: May 05, 2022

About this record

Access comprehensive regulatory information for "Helena" CSF Protein reagent 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 4e186052a6c75b5af9aacc38b806e28b and manufactured by HELENA BIOSCIENCES EUROPE. The authorized representative in Taiwan is SHANG LI INSTRUMENTS CO., LTD..

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