Taiwan FDA registration a3a9ee5117621039e551a173805282fa

"Helena" Serum Protein kit (Non-sterile)

TW: "海倫那" 血清蛋白試劑組 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·HELENA BIOSCIENCES EUROPE·Registered Oct 19, 2016 – Oct 19, 2021Expired
Registration details
Analysis ID
a3a9ee5117621039e551a173805282fa
License Form
Ministry of Health Medical Device Import No. 017099
Customs Code
DHA09401709907
Company information
Manufacturer Country
United Kingdom
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
Oct 19, 2016
Expiry Date
Oct 19, 2021
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About this record

Access comprehensive regulatory information for "Helena" 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 a3a9ee5117621039e551a173805282fa and manufactured by HELENA BIOSCIENCES EUROPE. The authorized representative in Taiwan is SHANG LI INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HELENA LABORATORIES CORP., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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