Pure Global

“Hong Shiang”eplilator (Non-Sterile) - Taiwan Registration d41090c2ab688188f7d82fd37bf79b67

Access comprehensive regulatory information for “Hong Shiang”eplilator (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 d41090c2ab688188f7d82fd37bf79b67 and manufactured by HONG SHIANG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is HONG SHIANG TECHNOLOGY 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
d41090c2ab688188f7d82fd37bf79b67
Registration Details
Taiwan FDA Registration: d41090c2ab688188f7d82fd37bf79b67
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Hong Shiang”eplilator (Non-Sterile)
TW: “鴻祥”除毛機(未滅菌)
Risk Class 1
MD

Registration Details

d41090c2ab688188f7d82fd37bf79b67

Ministry of Health Medical Device Manufacturing No. 009051

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Probe Hair Removal Machine (I.5350)".

I General and plastic surgical devices

I5350 Probe Hair Remover

Produced in Taiwan, China

Dates and Status

Apr 23, 2021

Apr 23, 2026