Taiwan FDA registration d08b9a6d0aa19d51c039f90c1880d77b

"Siemens" X-ray system for whole body diagnostics

TW: “西門子”全身診斷用X光系統
Taiwan flagTaiwan·Risk Class 2·Siemens Healthineers AG, X-Ray Products (XP)·Registered Feb 21, 2017 – Feb 21, 2027Active
Registration details
Analysis ID
d08b9a6d0aa19d51c039f90c1880d77b
Customs Code
DHAS5602939502
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.1650 透視X光影像增感管
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
Feb 21, 2017
Expiry Date
Feb 21, 2027
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About this record

Access comprehensive regulatory information for "Siemens" X-ray system for whole body diagnostics in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d08b9a6d0aa19d51c039f90c1880d77b and manufactured by Siemens Healthineers AG, X-Ray Products (XP). 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 AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP, Siemens Healthineers AG, X-Ray Products (XP), and 4 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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