Taiwan FDA registration f08bc8347ca375b974491b3b786455af
"McKovei" retrograde cardiac anesthesia catheter
TW: “邁柯唯”逆行性心臟麻醉導管
Taiwan·Risk Class 2·MAQUET CARDIOPLUMONARY MEDIKAL TEKNIK SAN. TIC LTD. STI;; MAQUET CARDIOPULMONARY AG·Registered Jun 26, 2009 – Jun 26, 2019CancelledRegistration details
- Analysis ID
- f08bc8347ca375b974491b3b786455af
- Customs Code
- DHA00601992804
Company information
- Manufacturer Country
- Türkiye;;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.4210 Vascular catheters, cannulas and tubes for cardiopulmonary vascular bypassing
- Import Information
- import
Dates and status
- Registration Date
- Jun 26, 2009
- Expiry Date
- Jun 26, 2019
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "McKovei" retrograde cardiac anesthesia catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f08bc8347ca375b974491b3b786455af and manufactured by MAQUET CARDIOPLUMONARY MEDIKAL TEKNIK SAN. TIC LTD. STI;; MAQUET CARDIOPULMONARY AG. 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