Pure Global

"R-Biopharm" Entamoeba histolytica IgG ELISA kit (Non-Sterile) - Taiwan Registration 3ce4d6d0041b6ecdbad4feea46b8b5a3

Access comprehensive regulatory information for "R-Biopharm" Entamoeba histolytica IgG ELISA 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 3ce4d6d0041b6ecdbad4feea46b8b5a3 and manufactured by R-BIOPHARM AG. The authorized representative in Taiwan is TRUGENE DIAGNOSTICS, INC..

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
3ce4d6d0041b6ecdbad4feea46b8b5a3
Registration Details
Taiwan FDA Registration: 3ce4d6d0041b6ecdbad4feea46b8b5a3
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"R-Biopharm" Entamoeba histolytica IgG ELISA kit (Non-Sterile)
TW: "ๅ…ซๆ–น" ็—ข็–พ้˜ฟ็ฑณๅทดๅ…็–ซๆชข้ฉ—่ฉฆๅŠ‘็ต„ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

3ce4d6d0041b6ecdbad4feea46b8b5a3

Ministry of Health Medical Device Import No. 013761

DHA09401376103

Company Information

Germany

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Dysentery Amoeba Sera Reagent (C.3220)".

C Immunology and microbiology devices

C3220 Dysentery amoeba serum reagent

Imported from abroad

Dates and Status

Jan 08, 2014

Jan 08, 2024