"McKovei" double vena vein drainage perfusion catheter
Taiwan·Risk Class 2·MAQUET CARDIOPLUMONARY MEDIKAL TEKNIK SAN. TIC LTD. STI;; MAQUET CARDIOPULMONARY AG·Registered Jan 18, 2010 – Jan 18, 2020Cancelled- Analysis ID
- 3cb6e2f2cb38b1794ce788ea71cc7e0d
- Customs Code
- DHA00602053409
- Manufacturer Country
- Türkiye;;Germany
- Authorized Representative
- GETINGE GROUP TAIWAN CO., LTD.
- 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
- Registration Date
- Jan 18, 2010
- Expiry Date
- Jan 18, 2020
- Cancellation Date
- Jun 16, 2022
- Status
- Logged out
- Reason
- 自行鍵入
Access comprehensive regulatory information for "McKovei" double vena vein drainage perfusion catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3cb6e2f2cb38b1794ce788ea71cc7e0d 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.