Taiwan FDA registration ea383c231ee8240e2f855136be691acb
“Philips” Quantification Software
TW: “飛利浦” 定量軟體
Taiwan·Risk Class 2·MD·Philips Ultrasound, LLC·Registered Oct 21, 2014 – Oct 21, 2024ExpiredRegistration details
- Analysis ID
- ea383c231ee8240e2f855136be691acb
- License Form
- Ministry of Health Medical Device Import No. 026591
- Customs Code
- DHA05602659105
Company information
- Manufacturer
- Philips Ultrasound, LLC
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN 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)
- P2050 Medical Image Management and Processing System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 21, 2014
- Expiry Date
- Oct 21, 2024
About this record
Access comprehensive regulatory information for “Philips” Quantification Software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ea383c231ee8240e2f855136be691acb and manufactured by Philips Ultrasound, LLC. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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