Taiwan FDA registration 7c9bf591632fb8cb91b586eb4ff03672

“ZIEHM” Mobile C-arm X-ray System

TW: “希姆”移動式C型臂X光機
Taiwan flagTaiwan·Risk Class 2·MD·Ziehm Imaging GmbH·Registered Jun 08, 2017 – Jun 08, 2027Active
Registration details
Analysis ID
7c9bf591632fb8cb91b586eb4ff03672
License Form
Ministry of Health Medical Device Import No. 029786
Customs Code
DHAS5602978604
Company information
Manufacturer
Ziehm Imaging GmbH
Manufacturer Country
Germany
Authorized Representative
PROMEDICS TECHNOLOGY CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
P Devices for radiology
Product Type (Level 2)
P1720 Mobile X-ray System
Import Information
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
Registration Date
Jun 08, 2017
Expiry Date
Jun 08, 2027
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About this record

Access comprehensive regulatory information for “ZIEHM” Mobile C-arm X-ray System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7c9bf591632fb8cb91b586eb4ff03672 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, 2 companies making similar products including Ziehm Imaging GmbH, Ziehn Imaging GmbH, and 5 recent registrations in the same category. 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.

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