Taiwan FDA registration 1bfda56cdb1a7951ef29fde905285758
“SIEMENS” Hemodynamic and Electrophysiological Recording system
TW: “西門子”血流動力及電生理紀錄系統
Taiwan·Risk Class 2·MD·Siemens Healthcare GmbH, Advanced Therapies·Registered Aug 31, 2017 – Aug 31, 2027ActiveRegistration details
- Analysis ID
- 1bfda56cdb1a7951ef29fde905285758
- License Form
- Ministry of Health Medical Device Import No. 030172
- Customs Code
- DHA05603017200
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)
- E Cardiovascular devices
- Product Type (Level 2)
- E1425 Programmable diagnostic PC
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 31, 2017
- Expiry Date
- Aug 31, 2027
About this record
Access comprehensive regulatory information for “SIEMENS” Hemodynamic and Electrophysiological Recording system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1bfda56cdb1a7951ef29fde905285758 and manufactured by Siemens Healthcare GmbH, Advanced Therapies. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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