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"Atrien" vascular tunneler (unsterilized) - Taiwan Registration 7bf83dcc72002d88a43a4b9acf19bbcf

Access comprehensive regulatory information for "Atrien" vascular tunneler (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7bf83dcc72002d88a43a4b9acf19bbcf and manufactured by ATRIUM MEDICAL CORPORATION. The authorized representative in Taiwan is GETINGE GROUP TAIWAN 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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7bf83dcc72002d88a43a4b9acf19bbcf
Registration Details
Taiwan FDA Registration: 7bf83dcc72002d88a43a4b9acf19bbcf
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Device Details

"Atrien" vascular tunneler (unsterilized)
TW: โ€œไบž็ฟ ๆฉโ€่ก€็ฎก้šง้“ๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

7bf83dcc72002d88a43a4b9acf19bbcf

DHA04400719902

Company Information

United States

Product Details

Limited to the first level identification range of medical equipment management measures for cardiovascular surgical instruments (E.4500).

E Cardiovascular Medicine Science

E.4500 ๅฟƒ่‡Ÿ่ก€็ฎกๅค–็ง‘ๅ™จๆขฐ

import

Dates and Status

Oct 31, 2008

Oct 31, 2018

Jun 16, 2022

Cancellation Information

Logged out

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