"Philips" ultrasonic system
- Analysis ID
- 00aa196f4fa4d3269179a2458d242ebf
- Customs Code
- DHA00602183900
- Manufacturer
- PHILIPS ULTRASOUND, INC.
- 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
- Dec 14, 2010
- Expiry Date
- Dec 14, 2025
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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 00aa196f4fa4d3269179a2458d242ebf and manufactured by PHILIPS ULTRASOUND, INC.. 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.