Taiwan FDA registration e75850c9b9589634d0864aef29e3b571

"McCove" bubble filter

TW: “邁柯唯”氣泡過濾器
Taiwan flagTaiwan·Risk Class 2·MAQUET Cardiopulmonary Medikal Teknik San. Twitch. Ltd. Sti;; MAQUET CARDIOPULMONARY AG·Registered May 07, 2011 – May 07, 2021Cancelled
Registration details
Analysis ID
e75850c9b9589634d0864aef29e3b571
Customs Code
DHA00602230606
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.4230 心臟血管繞道術之氣泡移除器
Import Information
import
Dates and status
Registration Date
May 07, 2011
Expiry Date
May 07, 2021
Cancellation Date
Aug 28, 2023
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "McCove" bubble filter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e75850c9b9589634d0864aef29e3b571 and manufactured by MAQUET Cardiopulmonary Medikal Teknik San. Twitch. 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, 1 companies making similar products including MAQUET CARDIOPLUMONARY MEDIKAL TEKNIK SAN. TIC LTD. STI;; Maquet Cardiopulmonary GmbH, and 1 recent registrations in the same category. 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.

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