Taiwan FDA registration fdb855ebb9615ad03d73e8f3b007498e
"McKovei" arteriovenous catheter
TW: “邁柯唯”動靜脈導管
Taiwan·Risk Class 2·MAQUET Cardiopulmonary Medikal Teknik San. Twitch. Ltd. Sti;; Maquet Cardiopulmonary GmbH·Registered Nov 03, 2010 – Nov 03, 2025ExpiredRegistration details
- Analysis ID
- fdb855ebb9615ad03d73e8f3b007498e
- Customs Code
- DHA00602163303
Company information
- Manufacturer
- MAQUET Cardiopulmonary Medikal Teknik San. Twitch. Ltd. Sti;; Maquet Cardiopulmonary GmbH
- 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
- Nov 03, 2010
- Expiry Date
- Nov 03, 2025
About this record
Access comprehensive regulatory information for "McKovei" arteriovenous catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fdb855ebb9615ad03d73e8f3b007498e and manufactured by MAQUET Cardiopulmonary Medikal Teknik San. Twitch. Ltd. Sti;; 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