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“BIOTRONIK”Magmaris Sirolimus-Eluting Resorbable Coronary Magnesium Scaffold System - Taiwan Registration e17465a1de1e3ea8b9fdcb68e8ceb217

Access comprehensive regulatory information for “BIOTRONIK”Magmaris Sirolimus-Eluting Resorbable Coronary Magnesium Scaffold System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number e17465a1de1e3ea8b9fdcb68e8ceb217 and manufactured by BIOTRONIK AG. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.

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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e17465a1de1e3ea8b9fdcb68e8ceb217
Registration Details
Taiwan FDA Registration: e17465a1de1e3ea8b9fdcb68e8ceb217
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Device Details

“BIOTRONIK”Magmaris Sirolimus-Eluting Resorbable Coronary Magnesium Scaffold System
TW: “百多力”鎂瑪斯西羅莫司冠狀動脈鎂金屬全吸收式支架系統
Risk Class 3
MD

Registration Details

e17465a1de1e3ea8b9fdcb68e8ceb217

Ministry of Health Medical Device Import No. 030827

DHA05603082700

Company Information

Switzerland

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular devices

E0001 Cardiovascular stents

Imports outside the borders;; Safety monitoring

Dates and Status

Oct 02, 2018

Oct 02, 2028