Taiwan FDA registration c93fef9da2cf0ff38094582979bf97b7

"Siemens" X-ray diagnostic system

TW: “西門子”X光診斷系統
Taiwan flagTaiwan·Risk Class 2·SIEMENS AG MEDICAL SOLUTIONS, BUSINESS UNIT XP·Registered Dec 24, 2012 – Dec 24, 2017Cancelled
Registration details
Analysis ID
c93fef9da2cf0ff38094582979bf97b7
Customs Code
DHAS0602427003
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
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
Dec 24, 2012
Expiry Date
Dec 24, 2017
Cancellation Date
Nov 04, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Siemens" X-ray 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 c93fef9da2cf0ff38094582979bf97b7 and manufactured by SIEMENS AG MEDICAL SOLUTIONS, BUSINESS UNIT XP. 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 SHANGHAI MEDICAL EQUIPMENT LTD., SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.;; Siemens Healthcare GmbH, X-Ray Products (XP), and 3 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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