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Bosch Transcatheter Pulmonary Valve System - Taiwan Registration dfca4e02e3f49d8c5ec841d3b21ed207

Access comprehensive regulatory information for Bosch Transcatheter Pulmonary Valve System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number dfca4e02e3f49d8c5ec841d3b21ed207 and manufactured by TAEWOONG MEDICAL CO., LTD.. The authorized representative in Taiwan is Xintech 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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dfca4e02e3f49d8c5ec841d3b21ed207
Registration Details
Taiwan FDA Registration: dfca4e02e3f49d8c5ec841d3b21ed207
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Device Details

Bosch Transcatheter Pulmonary Valve System
TW: ๆŸไธ–ๅคง็ถ“ๅฐŽ็ฎก่‚บๅ‹•่„ˆ็“ฃ่†œ็ณป็ตฑ
Risk Class 3

Registration Details

dfca4e02e3f49d8c5ec841d3b21ed207

DHA05603462709

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.3925 Hypocardial membrane substitutions

Safety monitoring;; import

Dates and Status

Dec 20, 2022

Dec 20, 2027