Pure Global

"Fisomer" multifunctional electrical stimulator - Taiwan Registration b252530f6e741142138ed1e106e1ab89

Access comprehensive regulatory information for "Fisomer" multifunctional electrical stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b252530f6e741142138ed1e106e1ab89 and manufactured by PHYSIOMED ELEKTROMEDIZIN AG. The authorized representative in Taiwan is GIGA MEDICAL INSTRUMENT 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
b252530f6e741142138ed1e106e1ab89
Registration Details
Taiwan FDA Registration: b252530f6e741142138ed1e106e1ab89
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Fisomer" multifunctional electrical stimulator
TW: "่ฒ็ดข็พŽ"ๅคšๅŠŸ่ƒฝ้›ปๅˆบๆฟ€ๅ™จ
Risk Class 2
Cancelled

Registration Details

b252530f6e741142138ed1e106e1ab89

DHA00601662602

Company Information

Germany

Product Details

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

K Neuroscience

import

Dates and Status

Jun 05, 2006

Jun 05, 2021

Aug 15, 2023

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ