Pure Global

“ALIFAX” Automated sedimentation rate device (Non-sterile) - Taiwan Registration 931ce38adc4fd03454a67d1b29889da2

Access comprehensive regulatory information for “ALIFAX” Automated sedimentation rate device (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 931ce38adc4fd03454a67d1b29889da2 and manufactured by Alifax S.r.l.. The authorized representative in Taiwan is SYSMEX TAIWAN 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
931ce38adc4fd03454a67d1b29889da2
Registration Details
Taiwan FDA Registration: 931ce38adc4fd03454a67d1b29889da2
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“ALIFAX” Automated sedimentation rate device (Non-sterile)
TW: "希森美康"全自動紅血球沉降速率儀(未滅菌)
Risk Class 1
MD

Registration Details

931ce38adc4fd03454a67d1b29889da2

Ministry of Health Medical Device Import No. 014238

DHA09401423806

Company Information

Italy

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Automatic Sedimentation Rate Device (B.5800)".

B Hematology and pathology devices

B5800 Automatic Settling Rate Device

Imported from abroad

Dates and Status

Jun 12, 2014

Jun 12, 2024