Taiwan FDA registration 0dfae6fe4776f2b0f847efcfddd82a6c

"Siemens" angiography system

TW: “西門子”血管攝影系統
Taiwan flagTaiwan·Risk Class 2·Siemens Healthcare GmbH, Advanced Therapies·Registered Aug 13, 2014 – Aug 13, 2019Cancelled
Registration details
Analysis ID
0dfae6fe4776f2b0f847efcfddd82a6c
Customs Code
DHAS5602643104
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.1600 X光血管攝影系統
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 13, 2014
Expiry Date
Aug 13, 2019
Cancellation Date
May 19, 2022
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

Access comprehensive regulatory information for "Siemens" angiography system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0dfae6fe4776f2b0f847efcfddd82a6c 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, 3 companies making similar products including Siemens Healthineers AG, Advanced Therapies, SIEMENS SHENZHEN MAGNETIC RESONANCE LTD., and 5 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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