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KatiaTM Chlamydomydia trachomatis IgA antibody detection panel - Taiwan Registration 862d48b5bd4f0a2ec2cf0488e975e392

Access comprehensive regulatory information for KatiaTM Chlamydomydia trachomatis IgA antibody detection panel in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 862d48b5bd4f0a2ec2cf0488e975e392 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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862d48b5bd4f0a2ec2cf0488e975e392
Registration Details
Taiwan FDA Registration: 862d48b5bd4f0a2ec2cf0488e975e392
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Device Details

KatiaTM Chlamydomydia trachomatis IgA antibody detection panel
TW: ๅก่’‚้›…TMๆฒ™็œผๆŠซ่กฃ่ŒIgAๆŠ—้ซ”ๆชขๆธฌ่ฉฆๅŠ‘็ต„
Risk Class 1
Cancelled

Registration Details

862d48b5bd4f0a2ec2cf0488e975e392

DHA04400180705

Company Information

United States

Product Details

Detection of antibodies to Chlamydia antigen in human blood.

C Immunology and microbiology

import

Dates and Status

Nov 08, 2005

Nov 08, 2010

Nov 27, 2012

Cancellation Information

Logged out

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