Pure Global

“Chang Gung” Plinth (Non-Sterile) - Taiwan Registration 30050b42e9a72c7ac3d65a0df1d2b50a

Access comprehensive regulatory information for “Chang Gung” Plinth (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 30050b42e9a72c7ac3d65a0df1d2b50a and manufactured by Chang Gung Medical Technology Co., Ltd. Linkou Factory. The authorized representative in Taiwan is CHANG GUNG MEDICAL 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
30050b42e9a72c7ac3d65a0df1d2b50a
Registration Details
Taiwan FDA Registration: 30050b42e9a72c7ac3d65a0df1d2b50a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Chang Gung” Plinth (Non-Sterile)
TW: “長庚”治療檯 (未滅菌)
Risk Class 1
MD

Registration Details

30050b42e9a72c7ac3d65a0df1d2b50a

Ministry of Health Medical Device Manufacturing Registration No. 005457

Company Information

Taiwan, Province of China

Product Details

Limited to the first-level identification range of the Measures for the Administration of Medical Equipment "Treatment Table (O.3520)".

o Equipment for physical medicine

O3520 treatment unit

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2025