Taiwan FDA registration e2a969975d7855cb9bff309cfdd05abb

Mobile X-ray system "Siemens"

TW: “西門子”移動式X光系統
Taiwan flagTaiwan·Risk Class 2·Siemens Healthcare GmbH, Advanced Therapies·Registered Aug 14, 2019 – Aug 14, 2024Cancelled
Registration details
Analysis ID
e2a969975d7855cb9bff309cfdd05abb
Customs Code
DHAS9200106103
Company information
Manufacturer Country
Germany
Authorized Representative
SIEMENS HEALTHCARE LIMITED
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1730 照相透視X光系統
Import Information
Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and status
Registration Date
Aug 14, 2019
Expiry Date
Aug 14, 2024
Cancellation Date
Apr 15, 2020
Cancellation information
Status
Logged out
Reason
移轉(製造廠)
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About this record

Access comprehensive regulatory information for Mobile X-ray system "Siemens" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e2a969975d7855cb9bff309cfdd05abb and manufactured by Siemens Healthcare GmbH, Advanced Therapies. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Siemens Healthineers AG, Advanced Therapies, Siemens Healthcare GmbH;; SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD., and 3 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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