Taiwan FDA registration d20432180201169346b8e9e421500ca7
“ZIEHM” Mobile C-arm X-ray System (Hybrid)
TW: “希姆”移動式C型臂X光機
Taiwan·Risk Class 2·MD·Ziehm Imaging GmbH·Registered Apr 11, 2016 – Apr 11, 2026ExpiredRegistration details
- Analysis ID
- d20432180201169346b8e9e421500ca7
- License Form
- Ministry of Health Medical Device Import No. 028507
- Customs Code
- DHAS5602850708
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
- Apr 11, 2016
- Expiry Date
- Apr 11, 2026
About this record
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..
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