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"Bertie" thrombus clearance duct - Taiwan Registration 931654fc6f2b7700ca8378f18dc3db8f

Access comprehensive regulatory information for "Bertie" thrombus clearance duct in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 931654fc6f2b7700ca8378f18dc3db8f and manufactured by Bioptimal International Pte. Ltd.. The authorized representative in Taiwan is HSIN TUNG MEDICAL 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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931654fc6f2b7700ca8378f18dc3db8f
Registration Details
Taiwan FDA Registration: 931654fc6f2b7700ca8378f18dc3db8f
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Device Details

"Bertie" thrombus clearance duct
TW: "ๆŸ่’‚" ่ก€ๆ “ๆธ…้™คๅฐŽ็ฎก
Risk Class 2

Registration Details

931654fc6f2b7700ca8378f18dc3db8f

DHA00600901505

Company Information

Product Details

0608 Other intensive care units and cardiac intensive care room management

import

Dates and Status

Feb 01, 1999

Feb 01, 2029