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"Helena" Capillary Serum Protein kit (Non-Sterile) - Taiwan Registration 2f8144172023dfb4b1671ade6b15a3bd

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..

This page provides complete technical specifications, regulatory compliance details. 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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2f8144172023dfb4b1671ade6b15a3bd
Registration Details
Taiwan FDA Registration: 2f8144172023dfb4b1671ade6b15a3bd
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Device Details

"Helena" Capillary Serum Protein kit (Non-Sterile)
TW: "ๆตทๅ€ซ้‚ฃ" ๆฏ›็ดฐ็ฎก่ก€ๆธ…่›‹็™ฝ้›ปๆณณๅฅ—็ต„(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

2f8144172023dfb4b1671ade6b15a3bd

Ministry of Health Medical Device Import No. 018970

DHA09401897001

Company Information

United Kingdom

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Protein (Chemical Separation Method) Test System (A.1630)".

A Clinical chemistry and clinical toxicology

A1630 Protein (Chemical Separation) Test System

Imported from abroad

Dates and Status

Apr 16, 2018

Apr 16, 2023