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Ascyrus Medical Dissection Stent Hybrid Prosthesis - Taiwan Registration c7035e869bc5ffc504ebb3e82760619e

Access comprehensive regulatory information for Ascyrus Medical Dissection Stent Hybrid Prosthesis in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number c7035e869bc5ffc504ebb3e82760619e and manufactured by Ascyrus Medical GmbH. The authorized representative in Taiwan is DR SHAO MD REGULATORY CONSULTANTS 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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c7035e869bc5ffc504ebb3e82760619e
Registration Details
Taiwan FDA Registration: c7035e869bc5ffc504ebb3e82760619e
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Device Details

Ascyrus Medical Dissection Stent Hybrid Prosthesis
TW: ๆ„›ๆ€่ณฝ็‘žๆ–ฏ่ค‡ๅˆๅผไธปๅ‹•่„ˆๅ‰้›ขๆ”ฏๆžถ
Risk Class 3
MD

Registration Details

c7035e869bc5ffc504ebb3e82760619e

Ministry of Health Medical Device Import No. 035999

DHA05603599902

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E0001 Cardiovascular stents

Imported from abroad

Dates and Status

Jul 19, 2023

Jul 19, 2028