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“Quidel” Lyra Direct C. difficile Assay (Non-Sterile) - Taiwan Registration 7feea2cb3449fe6d4829c0107b7c02f1

Access comprehensive regulatory information for “Quidel” Lyra Direct C. difficile Assay (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7feea2cb3449fe6d4829c0107b7c02f1 and manufactured by QUIDEL CORPORATION. The authorized representative in Taiwan is BIO-CHECK LABORATORIES 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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7feea2cb3449fe6d4829c0107b7c02f1
Registration Details
Taiwan FDA Registration: 7feea2cb3449fe6d4829c0107b7c02f1
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Device Details

“Quidel” Lyra Direct C. difficile Assay (Non-Sterile)
TW: “快得利”萊拉困難梭狀芽孢桿菌分子檢測套組 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

7feea2cb3449fe6d4829c0107b7c02f1

Ministry of Health Medical Device Import No. 014812

DHA09401481202

Company Information

United States

Product Details

C Immunology and microbiology devices

C2660 Microbial identification and assay equipment

Imported from abroad

Dates and Status

Dec 31, 2014

Dec 31, 2019

Aug 05, 2022

Cancellation Information

Logged out

未展延而逾期者