Taiwan FDA registration 61076dcf229e1ea6b16e0202a9aca579
"Yuetinghe" cardiopulmonary bypass tubing set (with Bioline coating)
TW: “悅廷和” 體外循環管路組(含Bioline塗層)
Taiwan·Risk Class 3·Maquet Cardiopulmonary GmbH·Registered Jul 05, 2023 – Jul 05, 2028ActiveRegistration details
- Analysis ID
- 61076dcf229e1ea6b16e0202a9aca579
- Customs Code
- DHA05603656102
Company information
- Manufacturer
- Maquet Cardiopulmonary GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- GETINGE GROUP TAIWAN CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.4210 心肺血管繞道術之血管導管、套管及管子;; E.4350 心肺血管繞道術和氧器;; 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
- Jul 05, 2023
- Expiry Date
- Jul 05, 2028
About this record
Access comprehensive regulatory information for "Yuetinghe" cardiopulmonary bypass tubing set (with Bioline coating) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 61076dcf229e1ea6b16e0202a9aca579 and manufactured by 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