Taiwan FDA registration ae4f94d81a7e6c2950b8f69124a2b5f5
“SIEMENS” Diagnostic digital imaging system workstation
TW: “西門子”影像處理工作系統
Taiwan·Risk Class 2·MD·SIEMENS HEALTHCARE GMBH, ADVANCED THERAPIES·Registered Mar 25, 2016 – Mar 25, 2026ExpiredRegistration details
- Analysis ID
- ae4f94d81a7e6c2950b8f69124a2b5f5
- License Form
- Ministry of Health Medical Device Import No. 028271
- Customs Code
- DHA05602827100
Company information
- Manufacturer
- SIEMENS HEALTHCARE GMBH, ADVANCED THERAPIES
- 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 Devices for radiology
- Product Type (Level 2)
- P2050 Medical Image Management and Processing System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 25, 2016
- Expiry Date
- Mar 25, 2026
About this record
Access comprehensive regulatory information for “SIEMENS” Diagnostic digital imaging system workstation in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ae4f94d81a7e6c2950b8f69124a2b5f5 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