Taiwan FDA registration 4ba9fe518e748500ad7467c38ceb31b2

"Siemens" linear accelerator

TW: “西門子”直線加速器
Taiwan flagTaiwan·Risk Class 2·SIEMENS AG MEDICAL SOLUTIONS,BUSINESS UNIT CV·Registered Jun 30, 2009 – Jun 30, 2014Cancelled
Registration details
Analysis ID
4ba9fe518e748500ad7467c38ceb31b2
Customs Code
DHAS0601993407
Company information
Manufacturer Country
Germany
Authorized Representative
SIEMENS 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.5050 Medical Charged Particle Radiotherapy System
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
Jun 30, 2009
Expiry Date
Jun 30, 2014
Cancellation Date
Jul 31, 2018
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for "Siemens" linear accelerator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4ba9fe518e748500ad7467c38ceb31b2 and manufactured by SIEMENS AG MEDICAL SOLUTIONS,BUSINESS UNIT CV. The authorized representative in Taiwan is SIEMENS LIMITED.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Siemens AG, Medical Solutions, Business Unit CR Segment RO, SIEMENS AG MEDICAL SOLUTIONS, DIVISION CO, and 2 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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