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"Helena" QuickGel Serum Protein kit (Non-Sterile) - Taiwan Registration 0f51ffd0f42c90fb745fe4fb3c948fc4

Access comprehensive regulatory information for "Helena" QuickGel 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 0f51ffd0f42c90fb745fe4fb3c948fc4 and manufactured by HELENA LABORATORIES, INC.. 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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0f51ffd0f42c90fb745fe4fb3c948fc4
Registration Details
Taiwan FDA Registration: 0f51ffd0f42c90fb745fe4fb3c948fc4
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Device Details

"Helena" QuickGel Serum Protein kit (Non-Sterile)
TW: "่ณ€่“ฎ้‚ฃ" ่ก€ๆธ…่›‹็™ฝ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

0f51ffd0f42c90fb745fe4fb3c948fc4

Ministry of Health Medical Device Import No. 016858

DHA09401685807

Company Information

Japan

Product Details

Limited to the first level identification range of the total protein test system (A.1635) of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A1635 Total Protein Test System

Imported from abroad

Dates and Status

Aug 03, 2016

Aug 03, 2021