Taiwan FDA registration d2fc68428c71598a5a90e7556730f658

"Siemens" positron/computed tomography system

TW: “西門子”正子/電腦斷層掃描系統
Taiwan flagTaiwan·Risk Class 2·Siemens Medical Solutions USA, Inc·Registered Jun 20, 2018 – Jun 20, 2028Active
Registration details
Analysis ID
d2fc68428c71598a5a90e7556730f658
Customs Code
DHAS5603092301
Company information
Manufacturer Country
United States
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.1200 Radiology computed tomography system;; P.1750 Computed Tomography X-ray System
Import Information
Input;; The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". 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
Jun 20, 2018
Expiry Date
Jun 20, 2028
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About this record

Access comprehensive regulatory information for "Siemens" positron/computed tomography system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d2fc68428c71598a5a90e7556730f658 and manufactured by Siemens Medical Solutions USA, Inc. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Siemens Medical Solutions USA, Inc, Siemens Medical Solutions USA, Inc., 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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