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"Siemens" ultrasonic diagnostic system - Taiwan Registration bc2374323f5223eace31ed416d2ef32c

Access comprehensive regulatory information for "Siemens" ultrasonic diagnostic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bc2374323f5223eace31ed416d2ef32c and manufactured by PANASONIC HEALTHCARE CO., LTD.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including PANASONIC HEALTHCARE CO., LTD., SIEMENS MEDICAL SOLUTIONS USA, INC., and 3 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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bc2374323f5223eace31ed416d2ef32c
Registration Details
Taiwan FDA Registration: bc2374323f5223eace31ed416d2ef32c
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Device Details

"Siemens" ultrasonic diagnostic system
TW: โ€œ่ฅฟ้–€ๅญโ€่ถ…้Ÿณๆณข่จบๆ–ท็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

bc2374323f5223eace31ed416d2ef32c

DHA00601796602

Company Information

Product Details

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

P Radiology Science

P.1550 Ultrasonic pulsating Duppler imaging system

import

Dates and Status

Mar 28, 2007

Mar 28, 2017

Nov 04, 2019

Cancellation Information

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