Taiwan FDA registration c5640cf41e8ad7bd01b59504ec8cd5c1
“Siemens”Probe for medical use
TW: “西門子”診斷用超音波探頭
Taiwan·Risk Class 2·MD·Siemens Healthineers Ltd.·Registered Oct 22, 2009 – Oct 22, 2024ExpiredRegistration details
- Analysis ID
- c5640cf41e8ad7bd01b59504ec8cd5c1
- License Form
- Department of Health Medical Device Import No. 020247
- Customs Code
- DHA00602024706
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)
- P1570 Ultrasound converter for diagnostics
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 22, 2009
- Expiry Date
- Oct 22, 2024
About this record
Access comprehensive regulatory information for “Siemens”Probe for medical use in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c5640cf41e8ad7bd01b59504ec8cd5c1 and manufactured by Siemens Healthineers Ltd.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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