"Philips" ultrasonic system
Taiwan·Risk Class 2·Philips Healthcare (Suzhou) Co., Ltd;; Philips Ultrasound, LLC·Registered Mar 07, 2017 – Oct 18, 2028Active- Analysis ID
- 0b3a52e1b99a936ba5138f3076ed9aaf
- Customs Code
- DHA09200081808
- 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.1560 超音波回音影像系統
- Import Information
- Input;; Chinese goods;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.
- Registration Date
- Mar 07, 2017
- Expiry Date
- Oct 18, 2028
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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 0b3a52e1b99a936ba5138f3076ed9aaf 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.