Pure Global

"Medtronic" aortic prosthetic vascular valve - Taiwan Registration 63c50fc218629630657b6801668d1e25

Access comprehensive regulatory information for "Medtronic" aortic prosthetic vascular valve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 63c50fc218629630657b6801668d1e25 and manufactured by Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
63c50fc218629630657b6801668d1e25
Registration Details
Taiwan FDA Registration: 63c50fc218629630657b6801668d1e25
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Medtronic" aortic prosthetic vascular valve
TW: โ€œ็พŽๆ•ฆๅŠ›โ€ไธปๅ‹•่„ˆไบบๅทฅ่ก€็ฎก็“ฃ่†œ
Risk Class 3
Cancelled

Registration Details

63c50fc218629630657b6801668d1e25

DHA00602374001

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.3925 Hypocardial membrane substitutions

import

Dates and Status

Jun 26, 2012

Jun 26, 2017

Sep 23, 2015

Cancellation Information

Logged out

่‡ช่ซ‹่จป้Šท