Taiwan FDA registration ddb353d343cb89fdb94d4ebe8218d332

"Siemens" X-ray vascular diagnostic system

TW: "西門子"X光血管診斷系統
Taiwan flagTaiwan·Risk Class 2·SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.·Registered Sep 04, 2006 – Sep 04, 2016Cancelled
Registration details
Analysis ID
ddb353d343cb89fdb94d4ebe8218d332
Customs Code
DHAS4200014001
Company information
Manufacturer Country
China
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.1600 X光血管攝影系統
Import Information
Input;; Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); Chinese goods
Dates and status
Registration Date
Sep 04, 2006
Expiry Date
Sep 04, 2016
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" X-ray vascular diagnostic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ddb353d343cb89fdb94d4ebe8218d332 and manufactured by SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.. The authorized representative in Taiwan is SIEMENS LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD., and 1 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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