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KatiaTM ENA Joint Screening Group - Taiwan Registration 094d62352f7f22f187db635d65e1c0b5

Access comprehensive regulatory information for KatiaTM ENA Joint Screening Group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 094d62352f7f22f187db635d65e1c0b5 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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094d62352f7f22f187db635d65e1c0b5
Registration Details
Taiwan FDA Registration: 094d62352f7f22f187db635d65e1c0b5
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Device Details

KatiaTM ENA Joint Screening Group
TW: ๅก่’‚้›…TM ENA่ฏๅˆ็ฏฉ้ธ็ต„
Risk Class 2
Cancelled

Registration Details

094d62352f7f22f187db635d65e1c0b5

DHA00601727402

Company Information

United States

Product Details

Enzyme immunosorption analysis was used to detect ENA antigen 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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