“Philips” Affiniti Series Ultrasound System
Taiwan·Risk Class 2·MD·Philips Ultrasound, LLC·Registered Sep 14, 2021 – Sep 14, 2026Active- Analysis ID
- cac5a9fa998e4de0e42fc141f0b7d4c2
- License Form
- Ministry of Health Medical Device Import No. 034861
- Customs Code
- DHA05603486104
- Manufacturer
- Philips Ultrasound, LLC
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1550 ultrasonic pulsating Doppler imaging system
- Import Information
- Imported from abroad
- Registration Date
- Sep 14, 2021
- Expiry Date
- Sep 14, 2026
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Access comprehensive regulatory information for “Philips” Affiniti Series Ultrasound System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cac5a9fa998e4de0e42fc141f0b7d4c2 and manufactured by Philips Ultrasound, LLC. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including For use only by the Parts System Denda;;For spare parts system only;;Philips Ultrasound, LLC, and 1 recent registrations in the same category. 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.