Taiwan FDA registration e232108322884be00bb8d1e150e38f4e

"Siemens" cardiac catheterization evaluation workstation

TW: "西門子"心導管檢查評估工作站
Taiwan flagTaiwan·Risk Class 2·Siemens Healthcare GmbH, Advanced Therapies·Registered Apr 06, 2006 – Apr 06, 2026Expired
Registration details
Analysis ID
e232108322884be00bb8d1e150e38f4e
Customs Code
DHA00601423602
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
Import Information
import
Dates and status
Registration Date
Apr 06, 2006
Expiry Date
Apr 06, 2026
About this record

Access comprehensive regulatory information for "Siemens" cardiac catheterization evaluation workstation in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e232108322884be00bb8d1e150e38f4e and manufactured by Siemens Healthcare GmbH, Advanced Therapies. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details. 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.

Free DatabasePowered by Pure Global AI89,000+ Devices