Pure Global

"McCovi" centrifugal pump (including Bioline) - Taiwan Registration 4deb5d84763543ca6e093f89c948d2ab

Access comprehensive regulatory information for "McCovi" centrifugal pump (including Bioline) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 4deb5d84763543ca6e093f89c948d2ab and manufactured by Maquet Cardiopulmonary GmbH;; MAQUET Cardiopulmonary GmbH. The authorized representative in Taiwan is GETINGE GROUP TAIWAN 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
4deb5d84763543ca6e093f89c948d2ab
Registration Details
Taiwan FDA Registration: 4deb5d84763543ca6e093f89c948d2ab
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"McCovi" centrifugal pump (including Bioline)
TW: โ€œ้‚ๆŸฏๅ”ฏโ€้›ขๅฟƒๅนซๆตฆ(ๅซBioline)
Risk Class 3

Registration Details

4deb5d84763543ca6e093f89c948d2ab

DHA00602099009

Company Information

Product Details

Centrifugal pumps are used in artificial cardiopulmonary support systems during surgery, or cardiopulmonary bypass. Centrifugal pumps deliver blood within a defined flow range.

E Cardiovascular Medicine Science

import

Dates and Status

May 04, 2010

May 04, 2025