"Philips" ultrasonic system
Taiwan·Risk Class 2·Philips Ultrasound, LLC·Registered Mar 14, 2014 – Mar 14, 2024Expired- Analysis ID
- 8ce18bcb404c1ed9a330b8db909e90e8
- Customs Code
- DHA05602600403
- 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 Ultrasonic Echo Imaging System;; P.1570 Ultrasound converters for diagnostic use;; P.1550 Ultrasonic pulsating Duppler imaging system
- Import Information
- import
- Registration Date
- Mar 14, 2014
- Expiry Date
- Mar 14, 2024
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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 8ce18bcb404c1ed9a330b8db909e90e8 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.