"Philips" ultrasonic system
Taiwan·Risk Class 2·Philips Healthcare (Suzhou) Co., Ltd;; Philips Ultrasound, LLC·Registered Jan 10, 2017 – Sep 11, 2027Active- Analysis ID
- d51ab98c6acf7179b08eed83024e62f3
- Customs Code
- DHA09200081107
- Manufacturer Country
- United States;;China
- 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
- Chinese goods;; input
- Registration Date
- Jan 10, 2017
- Expiry Date
- Sep 11, 2027
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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 d51ab98c6acf7179b08eed83024e62f3 and manufactured by Philips Healthcare (Suzhou) Co., Ltd;; 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.