Taiwan FDA registration 3aa6a66999469992c1be029ef138df20

"Helena" Serum Protein Kit (Non-sterile)

TW: "海倫那" 血清蛋白試劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·HELENA LABORATORIES CORP.·Registered Mar 29, 2017 – Mar 29, 2027Active
Registration details
Analysis ID
3aa6a66999469992c1be029ef138df20
License Form
Ministry of Health Medical Device Import No. 017660
Customs Code
DHA09401766004
Company information
Manufacturer Country
United States
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
Mar 29, 2017
Expiry Date
Mar 29, 2027
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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 3aa6a66999469992c1be029ef138df20 and manufactured by HELENA LABORATORIES CORP.. 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 BIOSCIENCES EUROPE, 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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