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"Dybo" DIMA H. Pylori Antigen Test (Non-Sterile) - Taiwan Registration 10275b086ccd31d6287aa25fee8a0ebb

Access comprehensive regulatory information for "Dybo" DIMA H. Pylori Antigen Test (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 10275b086ccd31d6287aa25fee8a0ebb and manufactured by BIOSYNEX S.A.. 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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10275b086ccd31d6287aa25fee8a0ebb
Registration Details
Taiwan FDA Registration: 10275b086ccd31d6287aa25fee8a0ebb
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Device Details

"Dybo" DIMA H. Pylori Antigen Test (Non-Sterile)
TW: "ๅธๅš" ่ฟช็‘ชๅนฝ้–€่žบๆ—‹ๆกฟ่ŒๆŠ—ๅŽŸๆชขๆธฌ่ฉฆๅŠ‘็›’ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

10275b086ccd31d6287aa25fee8a0ebb

Ministry of Health Medical Device Import No. 015621

DHA09401562100

Company Information

France

Product Details

C Immunology and microbiology devices

C0003 Helicobacter serological reagent

Imported from abroad

Dates and Status

Aug 31, 2015

Aug 31, 2020

May 19, 2022

Cancellation Information

Logged out

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