Taiwan FDA registration fc20d1d766cdf343cd2d940b78e37c22

"Siemens" linear accelerator

TW: "西門子" 直線加速器
Taiwan flagTaiwan·Risk Class 2·Siemens AG, Medical Solutions, Business Unit CR Segment RO·Registered Nov 03, 2005 – Nov 03, 2015Cancelled
Registration details
Analysis ID
fc20d1d766cdf343cd2d940b78e37c22
Customs Code
DHAS0601291609
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
Import Information
Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input
Dates and status
Registration Date
Nov 03, 2005
Expiry Date
Nov 03, 2015
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 fc20d1d766cdf343cd2d940b78e37c22 and manufactured by Siemens AG, Medical Solutions, Business Unit CR Segment RO. 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 CV, 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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