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"Berlin Heart" mobile drive for Aesker ventricular assist device - Taiwan Registration d52fa647698dcc067451b8d4038a092d

Access comprehensive regulatory information for "Berlin Heart" mobile drive for Aesker ventricular assist device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d52fa647698dcc067451b8d4038a092d and manufactured by BERLIN HEART GMBH. The authorized representative in Taiwan is ANSON HEALTH CARE INC..

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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d52fa647698dcc067451b8d4038a092d
Registration Details
Taiwan FDA Registration: d52fa647698dcc067451b8d4038a092d
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Device Details

"Berlin Heart" mobile drive for Aesker ventricular assist device
TW: โ€œๆŸๆž—ๅฟƒ่‡Ÿโ€่‰พๆ–ฏ็ง‘ๅฟƒๅฎค่ผ”ๅŠฉ่ฃ็ฝฎ็”จ็งปๅ‹•ๅผ้ฉ…ๅ‹•ๅ™จ
Risk Class 3
Cancelled

Registration Details

d52fa647698dcc067451b8d4038a092d

DHA00602035904

Company Information

Germany

Product Details

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

E Cardiovascular Medicine Science

E.3545 ๅฟƒๅฎค่ก€็ฎก็นž้“่ก“(่ผ”ๅŠฉ)่ฃ็ฝฎ

import

Dates and Status

Aug 05, 2009

Aug 05, 2019

May 19, 2022

Cancellation Information

Logged out

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