Taiwan FDA registration f019096cb3fe00dd7a5f6a248ac0b03d

"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 Jan 15, 2020 – Jan 15, 2030Active
Registration details
Analysis ID
f019096cb3fe00dd7a5f6a248ac0b03d
Customs Code
DHAS5603321400
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 CT system
Import Information
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". Input;; 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
Jan 15, 2020
Expiry Date
Jan 15, 2030
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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 f019096cb3fe00dd7a5f6a248ac0b03d 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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