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"Dybo" IMMUNOQUICK TOX A/B (Non-Sterile) - Taiwan Registration 9eca01c2d7f88527c0ed433da32fbeb8

Access comprehensive regulatory information for "Dybo" IMMUNOQUICK TOX A/B (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 9eca01c2d7f88527c0ed433da32fbeb8 and manufactured by BIOSYNEX. The authorized representative in Taiwan is DYBO ENTERPRISE 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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9eca01c2d7f88527c0ed433da32fbeb8
Registration Details
Taiwan FDA Registration: 9eca01c2d7f88527c0ed433da32fbeb8
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Device Details

"Dybo" IMMUNOQUICK TOX A/B (Non-Sterile)
TW: "ๅธๅš" ่‹ฑ่ซพ้ญๅ›ฐ้›ฃๆขญ็‹€่Šฝๅญขๆกฟ่ŒA/Bๆฏ’็ด ๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘็ต„ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

9eca01c2d7f88527c0ed433da32fbeb8

Ministry of Health Medical Device Import No. 015716

DHA09401571608

Company Information

France

Product Details

C Immunology and microbiology devices

C2660 Microbial identification and assay equipment

Imported from abroad

Dates and Status

Oct 05, 2015

Oct 05, 2020

May 06, 2019

Cancellation Information

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