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"Philips" ultrasonic system - Taiwan Registration 164051ad51e8b37a40aef7659b92bb77

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 164051ad51e8b37a40aef7659b92bb77 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.

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164051ad51e8b37a40aef7659b92bb77
Registration Details
Taiwan FDA Registration: 164051ad51e8b37a40aef7659b92bb77
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Device Details

"Philips" ultrasonic system
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€่ถ…้Ÿณๆณข็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

164051ad51e8b37a40aef7659b92bb77

DHA00602390201

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

P Radiology Science

P.1560 Ultrasonic Echo Imaging System;; P.1570 Ultrasound converters for diagnostic use;; P.1550 Ultrasonic pulsating Duppler imaging system

import

Dates and Status

Jul 20, 2012

Jul 20, 2017

Dec 13, 2019

Cancellation Information

Logged out

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