Taiwan FDA registration 17116ab5622167e2173b77cfc5fcf91f

Mobile X-ray system "Siemens"

TW: “西門子”移動式X光系統
Taiwan flagTaiwan·Risk Class 2·Siemens Healthcare GmbH;; SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.·Registered May 15, 2017 – May 15, 2027Active
Registration details
Analysis ID
17116ab5622167e2173b77cfc5fcf91f
Customs Code
DHAS9200083401
Company information
Manufacturer Country
Germany;;China
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;; Chinese goods;; 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
May 15, 2017
Expiry Date
May 15, 2027
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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 17116ab5622167e2173b77cfc5fcf91f and manufactured by Siemens Healthcare GmbH;; SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.. 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, Advanced Therapies, 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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