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Pushen triiodothyroxine enzyme immunoassay kit - Taiwan Registration a61e2a9a862f368b768e3acaa7fd68a1

Access comprehensive regulatory information for Pushen triiodothyroxine enzyme immunoassay kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a61e2a9a862f368b768e3acaa7fd68a1 and manufactured by BioCheck, Inc.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..

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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a61e2a9a862f368b768e3acaa7fd68a1
Registration Details
Taiwan FDA Registration: a61e2a9a862f368b768e3acaa7fd68a1
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Device Details

Pushen triiodothyroxine enzyme immunoassay kit
TW: ๆ™ฎ็”Ÿไธ‰็ข˜็”ฒ็‹€่…บ็ด ้…ต็ด ๅ…็–ซๅˆ†ๆžๅฅ—็ต„
Risk Class 2

Registration Details

a61e2a9a862f368b768e3acaa7fd68a1

DHA00601784809

Company Information

United States

Product Details

Quantitative detection of the concentration of triiodothyroxine in human serum.

A Clinical chemistry and clinical toxicology

A.1710 Total triiodothyroxine test system

import

Dates and Status

Dec 20, 2006

Dec 20, 2026