"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.
Device Details
Registration Details
9eca01c2d7f88527c0ed433da32fbeb8
Ministry of Health Medical Device Import No. 015716
DHA09401571608
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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