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"Savyon" Helicobacter pylori Antigen Rapid Test (Non-Sterile) - Taiwan Registration 977ed0323dbec956d89a709ab7c3d205

Access comprehensive regulatory information for "Savyon" Helicobacter pylori Antigen Rapid 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 977ed0323dbec956d89a709ab7c3d205 and manufactured by SAVYON DIAGNOSTICS LTD.. The authorized representative in Taiwan is SEEKERS BIOMEDICAL CO., LTD..

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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977ed0323dbec956d89a709ab7c3d205
Registration Details
Taiwan FDA Registration: 977ed0323dbec956d89a709ab7c3d205
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Device Details

"Savyon" Helicobacter pylori Antigen Rapid Test (Non-Sterile)
TW: "่ณฝ็ถญ็ฟ" ๅนฝ้–€ๆกฟ่ŒๆŠ—ๅŽŸๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

977ed0323dbec956d89a709ab7c3d205

Ministry of Health Medical Device Import No. 018776

DHA09401877602

Company Information

Israel

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Helicobacter Serological Reagent (C.0003)".

C Immunology and microbiology devices

C0003 Helicobacter serological reagent

Imported from abroad

Dates and Status

Jan 30, 2018

Jan 30, 2028