Taiwan FDA registration b539030c4e671b4ce78c0fef8f0a65e0

"McCove" bubble filter

TW: “邁柯唯”氣泡過濾器
Taiwan flagTaiwan·Risk Class 2·MAQUET CARDIOPLUMONARY MEDIKAL TEKNIK SAN. TIC LTD. STI;; Maquet Cardiopulmonary GmbH·Registered May 20, 2009 – May 20, 2024Expired
Registration details
Analysis ID
b539030c4e671b4ce78c0fef8f0a65e0
Customs Code
DHA00601986404
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 20, 2009
Expiry Date
May 20, 2024
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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 b539030c4e671b4ce78c0fef8f0a65e0 and manufactured by MAQUET CARDIOPLUMONARY MEDIKAL TEKNIK SAN. TIC 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, 1 companies making similar products including MAQUET Cardiopulmonary Medikal Teknik San. Twitch. Ltd. Sti;; MAQUET CARDIOPULMONARY AG, 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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