Taiwan FDA registration dcb28993e7cdfbfc7eb90df6199cc114
“Siemens”Ultrasonic imaging System
TW: “西門子”診斷用超音波系統
Taiwan·Risk Class 2·MD·Siemens Healthineers Ltd.·Registered Mar 06, 2009 – Mar 06, 2024ExpiredRegistration details
- Analysis ID
- dcb28993e7cdfbfc7eb90df6199cc114
- License Form
- Department of Health Medical Device Import No. 019691
- Customs Code
- DHA00601969102
Company information
- Manufacturer
- Siemens Healthineers Ltd.
- Manufacturer Country
- Korea, Republic of
- 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)
- P1550 ultrasonic pulsating Doppler imaging system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 06, 2009
- Expiry Date
- Mar 06, 2024
About this record
Access comprehensive regulatory information for “Siemens”Ultrasonic imaging System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dcb28993e7cdfbfc7eb90df6199cc114 and manufactured by Siemens Healthineers Ltd.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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