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Bayer rapid thromptom catheter set - Taiwan Registration 77817372b1f5e4b4c8c1d95a5576e9ff

Access comprehensive regulatory information for Bayer rapid thromptom catheter set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 77817372b1f5e4b4c8c1d95a5576e9ff 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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77817372b1f5e4b4c8c1d95a5576e9ff
Registration Details
Taiwan FDA Registration: 77817372b1f5e4b4c8c1d95a5576e9ff
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Device Details

Bayer rapid thromptom catheter set
TW: โ€œๆ‹œ่€ณโ€ๅฟซๆท่ก€ๆ “ๆธ…้™คๅฐŽ็ฎก็ต„
Risk Class 2
Cancelled

Registration Details

77817372b1f5e4b4c8c1d95a5576e9ff

DHA00601982405

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

May 01, 2009

May 01, 2019

Aug 05, 2022

Cancellation Information

Logged out

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