Taiwan FDA registration 6962109ea7675e035caae436b7323f18
“Philips” 5000 Compact Series Ultrasound Systems
TW: “飛利浦” 超音波系統
Taiwan·Risk Class 2·MD·Philips Ultrasound, LLC·Registered Aug 13, 2023 – Aug 13, 2028ActiveRegistration details
- Analysis ID
- 6962109ea7675e035caae436b7323f18
- License Form
- Ministry of Health Medical Device Import No. 036577
- Customs Code
- DHA05603657704
Company information
- Manufacturer
- Philips Ultrasound, LLC
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P1550 ultrasonic pulsating Doppler imaging system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 13, 2023
- Expiry Date
- Aug 13, 2028
About this record
Access comprehensive regulatory information for “Philips” 5000 Compact Series Ultrasound Systems in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6962109ea7675e035caae436b7323f18 and manufactured by Philips Ultrasound, LLC. The authorized representative in Taiwan is PHILIPS TAIWAN 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