Taiwan FDA registration 20c942d18859f93291fc758c58efd6f2

"Siemens" diagnostic X-ray machine

TW: “西門子”診斷型X光機
Taiwan flagTaiwan·Risk Class 2·Siemens Healthcare GmbH, X-Ray Products (XP)·Registered Dec 20, 2019 – Nov 06, 2022Cancelled
Registration details
Analysis ID
20c942d18859f93291fc758c58efd6f2
Customs Code
DHAS5603307206
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.1680 固定式X光系統
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 20, 2019
Expiry Date
Nov 06, 2022
Cancellation Date
Apr 12, 2024
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" diagnostic X-ray machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 20c942d18859f93291fc758c58efd6f2 and manufactured by Siemens Healthcare GmbH, X-Ray Products (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 AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP, Siemens Healthcare GmbH;; SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD., and 4 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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