"Philips" ultrasonic system
Taiwan·Risk Class 2·Philips Ultrasound, LLC·Registered Aug 01, 2012 – Aug 01, 2027Active- Analysis ID
- bac592f37bf75fdc285640f669a21185
- Customs Code
- DHA00602391500
- 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.1560 超音波回音影像系統
- Import Information
- import
- Registration Date
- Aug 01, 2012
- Expiry Date
- Aug 01, 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 bac592f37bf75fdc285640f669a21185 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.