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“Helena” Urine Protein Kit (Non-sterile) - Taiwan Registration 9a99806bd1179b88d81024de74cd632e

Access comprehensive regulatory information for “Helena” Urine 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 9a99806bd1179b88d81024de74cd632e 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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9a99806bd1179b88d81024de74cd632e
Registration Details
Taiwan FDA Registration: 9a99806bd1179b88d81024de74cd632e
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Device Details

“Helena” Urine Protein Kit (Non-sterile)
TW: “賀蓮那”尿蛋白電泳試劑 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

9a99806bd1179b88d81024de74cd632e

Ministry of Health Medical Device Import No. 014044

DHA09401404406

Company Information

United States

Product Details

A Clinical chemistry and clinical toxicology

A1630 Protein (Chemical Separation) Test System

Imported from abroad

Dates and Status

Apr 11, 2014

Apr 11, 2019

Jun 16, 2022

Cancellation Information

Logged out

許可證已逾有效期未申請展延