Taiwan FDA registration 2f04f684d0603e94f7b3a63473253818
"Siemens" portable ultrasonic system
TW: “西門子”攜帶式超音波系統
Taiwan·Risk Class 2·SIEMENS MEDICAL SOLUTIONS USA, INC.;; PLEXUS MANUFACTURING SDN. BHD.·Registered Dec 26, 2008 – Dec 26, 2018CancelledRegistration details
- Analysis ID
- 2f04f684d0603e94f7b3a63473253818
- Customs Code
- DHA00601953307
Company information
- Manufacturer Country
- United States;;Malaysia
- Authorized Representative
- SIEMENS LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1550 Ultrasonic pulsating Duppler imaging system
- Import Information
- import
Dates and status
- Registration Date
- Dec 26, 2008
- Expiry Date
- Dec 26, 2018
- Cancellation Date
- Apr 10, 2020
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Siemens" portable ultrasonic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2f04f684d0603e94f7b3a63473253818 and manufactured by SIEMENS MEDICAL SOLUTIONS USA, INC.;; PLEXUS MANUFACTURING SDN. BHD.. The authorized representative in Taiwan is SIEMENS 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