Taiwan FDA registration 3d6d1c4a1e0a7459af2adbf210255851
"McVier" centrifugal pump (without heparin coating)
TW: “邁柯唯”離心幫浦(未含肝素塗層)
Registration details
- Analysis ID
- 3d6d1c4a1e0a7459af2adbf210255851
- Customs Code
- DHA00602009002
Company information
- Manufacturer Country
- Germany
- Authorized Representative
- GETINGE GROUP TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.4360 非滾筒式心肺血管繞道術血液循環幫浦
- Import Information
- import
Dates and status
- Registration Date
- Aug 03, 2009
- Expiry Date
- Aug 03, 2029
About this record
Access comprehensive regulatory information for "McVier" centrifugal pump (without heparin coating) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3d6d1c4a1e0a7459af2adbf210255851 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 DatabasePowered by Pure Global AI89,000+ Devices