Taiwan FDA registration ba8d7c3c5c38c300a9fb38ae4552e467

"Siemens" diagnostic X-ray machine

TW: “西門子”診斷型X光機
Taiwan flagTaiwan·Risk Class 2·Siemens Healthcare GmbH;; SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.·Registered Nov 06, 2017 – Nov 06, 2022Cancelled
Registration details
Analysis ID
ba8d7c3c5c38c300a9fb38ae4552e467
Customs Code
DHAS9200087808
Company information
Manufacturer Country
Germany;;China
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
Contract manufacturing;; Chinese goods;; input
Dates and status
Registration Date
Nov 06, 2017
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 ba8d7c3c5c38c300a9fb38ae4552e467 and manufactured by Siemens Healthcare GmbH;; SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.. 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, X-Ray Products (XP), 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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