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"Quidel" AmpliVue C. difficile Assay (Non-Sterile) - Taiwan Registration 82ba10f7c6afde002975830041242ca8

Access comprehensive regulatory information for "Quidel" AmpliVue 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 82ba10f7c6afde002975830041242ca8 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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82ba10f7c6afde002975830041242ca8
Registration Details
Taiwan FDA Registration: 82ba10f7c6afde002975830041242ca8
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Device Details

"Quidel" AmpliVue C. difficile Assay (Non-Sterile)
TW: "ๅฟซๅพ—ๅˆฉ" ๅ›ฐ้›ฃๆขญ็‹€่Šฝๅญขๆกฟ่Œๅˆ†ๅญๆชขๆธฌๅฅ—็ต„ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

82ba10f7c6afde002975830041242ca8

Ministry of Health Medical Device Import No. 014983

DHA09401498300

Company Information

United States

Product Details

C Immunology and microbiology devices

C2660 Microbial identification and assay equipment

Imported from abroad

Dates and Status

Mar 09, 2015

Mar 09, 2020

May 15, 2019

Cancellation Information

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