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Diagnostec Helicobacter Pylori Antigen Rapid Test Kit (Non-Sterile) - Taiwan Registration 0e6d8b31c345aec5f670cb2c0d4f9b3e

Access comprehensive regulatory information for Diagnostec Helicobacter Pylori Antigen Rapid Test 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 0e6d8b31c345aec5f670cb2c0d4f9b3e and manufactured by Jei Daniel(JD) Biotech Corp.. The authorized representative in Taiwan is REININGHUN DIAGNOSTICS BIOMEDICAL CORPORATION.

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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0e6d8b31c345aec5f670cb2c0d4f9b3e
Registration Details
Taiwan FDA Registration: 0e6d8b31c345aec5f670cb2c0d4f9b3e
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Device Details

Diagnostec Helicobacter Pylori Antigen Rapid Test Kit (Non-Sterile)
TW: ๅพทๅ…‹ๅนฝ้–€่žบๆ—‹ๆกฟ่Œๆชขๆธฌ่ฉฆๅŠ‘็›’ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

0e6d8b31c345aec5f670cb2c0d4f9b3e

Ministry of Health Medical Device Land Transport No. 002307

DHA09600230702

Company Information

Product Details

C Immunology and microbiology devices

C0003 Helicobacter serological reagent

Imported from abroad; Made in China

Dates and Status

Jan 12, 2015

Jan 12, 2020

Jun 16, 2022

Cancellation Information

Logged out

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