Pure Global

“ZIEHM” Mobile C-arm X-ray System (Hybrid) - Taiwan Registration d20432180201169346b8e9e421500ca7

Access comprehensive regulatory information for “ZIEHM” Mobile C-arm X-ray System (Hybrid) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d20432180201169346b8e9e421500ca7 and manufactured by Ziehm Imaging GmbH. The authorized representative in Taiwan is PROMEDICS 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
d20432180201169346b8e9e421500ca7
Registration Details
Taiwan FDA Registration: d20432180201169346b8e9e421500ca7
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“ZIEHM” Mobile C-arm X-ray System (Hybrid)
TW: “希姆”移動式C型臂X光機
Risk Class 2
MD

Registration Details

d20432180201169346b8e9e421500ca7

Ministry of Health Medical Device Import No. 028507

DHAS5602850708

Company Information

Germany

Product Details

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

P Devices for radiology

P1720 Mobile X-ray System

Imported from abroad; Consent must be attached to the input (each input must be supported by the consent of the Atomic Energy Commission)

Dates and Status

Apr 11, 2016

Apr 11, 2026