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KatiaTM thyroglobulin antibody test set - Taiwan Registration 374ec6194e276cf7d0081f0f4b182cdf

Access comprehensive regulatory information for KatiaTM thyroglobulin antibody test set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 374ec6194e276cf7d0081f0f4b182cdf and manufactured by TRINITY BIOTECH USA. The authorized representative in Taiwan is GRAND MARQUIS 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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374ec6194e276cf7d0081f0f4b182cdf
Registration Details
Taiwan FDA Registration: 374ec6194e276cf7d0081f0f4b182cdf
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Device Details

KatiaTM thyroglobulin antibody test set
TW: ๅก่’‚้›…TM็”ฒ็‹€่…บ็ƒ่›‹็™ฝๆŠ—้ซ”ๆชขๆธฌ่ฉฆๅŠ‘็ต„
Risk Class 2
Cancelled

Registration Details

374ec6194e276cf7d0081f0f4b182cdf

DHA00601727300

Company Information

United States

Product Details

Enzyme immunoadsorption assay was used to detect thyroglobulin antibody in human serum.

A Clinical chemistry and clinical toxicology

A.1685 Thyroxine-binding globulin testing system

import

Dates and Status

Aug 10, 2006

Aug 10, 2011

Nov 27, 2012

Cancellation Information

Logged out

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