Pure Global

"Astek" Portable IF Stimulator - Taiwan Registration 631c52be6765b423df69157988707d83

Access comprehensive regulatory information for "Astek" Portable IF Stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 631c52be6765b423df69157988707d83 and manufactured by ASTEK TECHNOLOGY LTD.. The authorized representative in Taiwan is ASTEK TECHNOLOGY 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
631c52be6765b423df69157988707d83
Registration Details
Taiwan FDA Registration: 631c52be6765b423df69157988707d83
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Astek" Portable IF Stimulator
TW: "ไบžๆ˜Ÿ"ๆ”œๅธถๅผไธญ้ ป้›ป็™‚ๅ™จ
Risk Class 2
MD

Registration Details

631c52be6765b423df69157988707d83

Ministry of Health Medical Device Manufacturing No. 005306

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

o Equipment for physical medicine

O5850 powered muscle stimulator

Produced in Taiwan, China

Dates and Status

Jan 26, 2016

Jan 26, 2026