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"Fujino" ultrasound endoscope - Taiwan Registration 5a70fa413eeec6b5e5a62a912abf3b97

Access comprehensive regulatory information for "Fujino" ultrasound endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5a70fa413eeec6b5e5a62a912abf3b97 and manufactured by FUJINON SANO CORPORATION. The authorized representative in Taiwan is WELMORE CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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5a70fa413eeec6b5e5a62a912abf3b97
Registration Details
Taiwan FDA Registration: 5a70fa413eeec6b5e5a62a912abf3b97
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Device Details

"Fujino" ultrasound endoscope
TW: โ€œๅฏŒๅฃซ่ƒฝโ€่ถ…้Ÿณๆณขๅ…ง่ฆ–้ก
Risk Class 2
Cancelled

Registration Details

5a70fa413eeec6b5e5a62a912abf3b97

DHA00601885600

Company Information

Japan

Product Details

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

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

May 14, 2008

May 14, 2013

Aug 03, 2015

Cancellation Information

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