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"Bayer" Ascot thrombus removal catheter group - Taiwan Registration 169ebb9aaa6ad4ed74b418c12b06db3c

Access comprehensive regulatory information for "Bayer" Ascot thrombus removal catheter group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 169ebb9aaa6ad4ed74b418c12b06db3c 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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169ebb9aaa6ad4ed74b418c12b06db3c
Registration Details
Taiwan FDA Registration: 169ebb9aaa6ad4ed74b418c12b06db3c
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Device Details

"Bayer" Ascot thrombus removal catheter group
TW: โ€œๆ‹œ่€ณโ€้›…ๅฃซ่ก€ๆ “ๆธ…้™คๅฐŽ็ฎก็ต„
Risk Class 2
Cancelled

Registration Details

169ebb9aaa6ad4ed74b418c12b06db3c

DHA00601972401

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

Mar 19, 2009

Mar 19, 2019

Aug 05, 2022

Cancellation Information

Logged out

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