"Philips" ultrasonic system
Taiwan·Risk Class 2·Neusoft Medical Systems Co., Ltd·Registered Aug 25, 2022 – Aug 25, 2027Active- Analysis ID
- 2e52032454a5a5145cdc575d18129f87
- Customs Code
- DHA09200138100
- Manufacturer
- Neusoft Medical Systems Co., Ltd
- Manufacturer Country
- China
- Authorized Representative
- PHILIPS TAIWAN LIMITED
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1550 Ultrasonic pulsating Duppler imaging system
- Import Information
- Input;; Chinese goods
- Registration Date
- Aug 25, 2022
- Expiry Date
- Aug 25, 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 2e52032454a5a5145cdc575d18129f87 and manufactured by Neusoft Medical Systems Co., Ltd. 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.