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"QIAGEN" artus c. difficile QS-RGQ MDx Kit (Non-sterile) - Taiwan Registration 2800ec9eb1394f7c61224a754a4adf19

Access comprehensive regulatory information for "QIAGEN" artus c. difficile QS-RGQ MDx Kit (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 2800ec9eb1394f7c61224a754a4adf19 and manufactured by QIAGEN GMBH. The authorized representative in Taiwan is QIAGEN TAIWAN COMPANY LIMITED.

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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2800ec9eb1394f7c61224a754a4adf19
Registration Details
Taiwan FDA Registration: 2800ec9eb1394f7c61224a754a4adf19
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Device Details

"QIAGEN" artus c. difficile QS-RGQ MDx Kit (Non-sterile)
TW: "ๅ‡ฑๆฐ" ้˜ฟ็‰นๆ–ฏๅ›ฐ้›ฃๆขญ็‹€่Šฝๅญขๆกฟ่Œๆชข้ฉ—่ฉฆๅŠ‘็ต„ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

2800ec9eb1394f7c61224a754a4adf19

Ministry of Health Medical Device Import No. 015549

DHA09401554902

Company Information

Germany

Product Details

C Immunology and microbiology devices

C2660 Microbial identification and assay equipment

Imported from abroad

Dates and Status

Aug 04, 2015

Aug 04, 2020

May 06, 2019

Cancellation Information

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