Bayer second-generation quick-take thrombus removal catheter - Taiwan Registration 7c01c42301d82e0ad6ab8cdc62d3afdc
Access comprehensive regulatory information for Bayer second-generation quick-take thrombus removal catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7c01c42301d82e0ad6ab8cdc62d3afdc 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.
Device Details
Product Details
For details, it is Chinese approved copy of the imitation order
E Cardiovascular Medicine Science
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import
Dates and Status
Jun 18, 2012
Jun 18, 2017
Dec 13, 2019
Cancellation Information
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