"Philips" ultrasonic system
Taiwan·Risk Class 2·Philips Ultrasound, LLC·Registered Mar 30, 2020 – Mar 30, 2030Active- Analysis ID
- 29a0f6a5cb4bc420ca7afc09f535edf2
- Customs Code
- DHA05603333800
- Manufacturer
- Philips Ultrasound, LLC
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
- 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
- Registration Date
- Mar 30, 2020
- Expiry Date
- Mar 30, 2030
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Access comprehensive regulatory information for "Philips" 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 29a0f6a5cb4bc420ca7afc09f535edf2 and manufactured by Philips Ultrasound, LLC. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including PHILIPS ULTRASOUND, INC., Philips Ultrasound, LLC, and 5 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.