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"Bayer" thrombus removal system - Taiwan Registration 43f58c703f4392caa0d0eec65616e918

Access comprehensive regulatory information for "Bayer" thrombus removal system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 43f58c703f4392caa0d0eec65616e918 and manufactured by Bayer Medical Care Inc.. The authorized representative in Taiwan is WATTCAN INSTRUMENTS 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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43f58c703f4392caa0d0eec65616e918
Registration Details
Taiwan FDA Registration: 43f58c703f4392caa0d0eec65616e918
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Device Details

"Bayer" thrombus removal system
TW: โ€œๆ‹œ่€ณโ€่ก€ๆ “ๆธ…้™ค็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

43f58c703f4392caa0d0eec65616e918

DHA00601989900

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.5150 ่ก€ๆ “ๅˆ‡้™ค่ก“ๅฐŽ็ฎก

import

Dates and Status

Jun 09, 2009

Jun 09, 2019

Aug 05, 2022

Cancellation Information

Logged out

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