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"McVi" Utima 2nd generation main chest dilator (unsterilized) - Taiwan Registration 76205838b8ee147af930bb930fb07afd

Access comprehensive regulatory information for "McVi" Utima 2nd generation main chest dilator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 76205838b8ee147af930bb930fb07afd and manufactured by MAQUET PUERTO RICO INC.. The authorized representative in Taiwan is RAYING TECHNOLOGY COMPANY.

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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76205838b8ee147af930bb930fb07afd
Registration Details
Taiwan FDA Registration: 76205838b8ee147af930bb930fb07afd
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Device Details

"McVi" Utima 2nd generation main chest dilator (unsterilized)
TW: โ€œ้‚ๆŸฏๅ”ฏโ€็ƒๆ้ฆฌ็ฌฌไบŒไปฃไธป่ƒธๆ“ดๅผตๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

76205838b8ee147af930bb930fb07afd

DHA04400415401

Company Information

United States

Product Details

It is limited to the scope of first-class identification of cardiovascular surgical devices (E.4500) in the Measures for the Administration of Medical Devices

E Cardiovascular Medicine Science

E.4500 ๅฟƒ่‡Ÿ่ก€็ฎกๅค–็ง‘ๅ™จๆขฐ

import

Dates and Status

Apr 21, 2006

Apr 21, 2011

Nov 16, 2012

Cancellation Information

Logged out

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