Taiwan FDA registration 04a6bb5a96c46c24caaf1e5c36b51965

"McVier" anterograde cardiac anesthesia catheter

TW: “邁柯唯”順行性心臟麻醉導管

Taiwan·Risk Class 2·MAQUET CARDIOPLUMONARY MEDIKAL TEKNIK SAN. TIC LTD. STI;; MAQUET CARDIOPULMONARY AG·Registered Apr 15, 2009 – Apr 15, 2019Cancelled

Registration details

Analysis ID: 04a6bb5a96c46c24caaf1e5c36b51965
Customs Code: DHA00601978100

Company information

Manufacturer: MAQUET CARDIOPLUMONARY MEDIKAL TEKNIK SAN. TIC LTD. STI;; MAQUET CARDIOPULMONARY AG
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: Apr 15, 2009
Expiry Date: Apr 15, 2019
Cancellation Date: Jun 16, 2022

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "McVier" anterograde 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 04a6bb5a96c46c24caaf1e5c36b51965 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.