Pure Global

"Kedir" cardiovascular surgical instrument (unsterilized) - Taiwan Registration 55bed855431600b4dc7f8a68130836ee

Access comprehensive regulatory information for "Kedir" cardiovascular surgical instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 55bed855431600b4dc7f8a68130836ee and manufactured by CARDIOMEDICAL 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
55bed855431600b4dc7f8a68130836ee
Registration Details
Taiwan FDA Registration: 55bed855431600b4dc7f8a68130836ee
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Kedir" cardiovascular surgical instrument (unsterilized)
TW: โ€œๅ‡ฑๅธ็ˆพโ€ๅฟƒ่‡Ÿ่ก€็ฎกๅค–็ง‘ๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

55bed855431600b4dc7f8a68130836ee

DHA04400441707

Company Information

Germany

Product Details

It is limited to the scope of first-class identification of cardiovascular surgical devices (E.4500) in the Measures for the Administration of Medical Devices.

E Cardiovascular Medicine Science

E.4500 ๅฟƒ่‡Ÿ่ก€็ฎกๅค–็ง‘ๅ™จๆขฐ

import

Dates and Status

May 10, 2006

May 10, 2011

Dec 03, 2012

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ