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KatiaTM Anti-Nuclear Antibody Detection Set - Taiwan Registration b26400b8f85815c5a99fee3dc5b61c67

Access comprehensive regulatory information for KatiaTM Anti-Nuclear Antibody Detection Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b26400b8f85815c5a99fee3dc5b61c67 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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b26400b8f85815c5a99fee3dc5b61c67
Registration Details
Taiwan FDA Registration: b26400b8f85815c5a99fee3dc5b61c67
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Device Details

KatiaTM Anti-Nuclear Antibody Detection Set
TW: ๅก่’‚้›…TM ๆŠ—็ดฐ่ƒžๆ ธๆŠ—้ซ”ๆชขๆธฌ่ฉฆๅŠ‘็ต„
Risk Class 2
Cancelled

Registration Details

b26400b8f85815c5a99fee3dc5b61c67

DHA00601727106

Company Information

United States

Product Details

Enzyme immunosorption assay was used to detect anti-nuclear antibodies in human serum.

C Immunology and microbiology

C.5100 ๆŠ—ๆ ธๆŠ—้ซ”ๅ…็–ซ่ฉฆ้ฉ—็ณป็ตฑ

import

Dates and Status

Aug 10, 2006

Aug 10, 2011

Nov 27, 2012

Cancellation Information

Logged out

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