Taiwan FDA registration f01525ba029fec32f1709c557cbb7721
"Siemens" magnetic resonance camera
TW: "西門子" 磁共振攝影機
Taiwan·Risk Class 2·Siemens Healthcare GmbH, Magnetic Resonance (MR)·Registered Nov 11, 2005 – Nov 11, 2020CancelledRegistration details
- Analysis ID
- f01525ba029fec32f1709c557cbb7721
- Customs Code
- DHA00601354500
Company information
- Manufacturer
- Siemens Healthcare GmbH, Magnetic Resonance (MR)
- 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
- Nov 11, 2005
- Expiry Date
- Nov 11, 2020
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Siemens" magnetic resonance camera in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f01525ba029fec32f1709c557cbb7721 and manufactured by Siemens Healthcare GmbH, Magnetic Resonance (MR). 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