Taiwan FDA registration 5054232b45c9079401931f0be5048cc0

"Mekewei" microporous membrane oxygenator with venous hard shell blood storage tank

TW: “邁柯唯”微孔膜氧合器附靜脈硬殼式儲血槽
Taiwan flagTaiwan·Risk Class 2·Maquet Cardiopulmonary AG; MAQUET Cardiopulmonary Medikal Teknik San. Twitch. Ltd. Sti·Registered Dec 13, 2010 – Dec 13, 2025Expired
Registration details
Analysis ID
5054232b45c9079401931f0be5048cc0
Customs Code
DHA00602183604
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.4400 心肺血管繞道術血液儲存器;; E.4350 心肺血管繞道術和氧器
Import Information
import
Dates and status
Registration Date
Dec 13, 2010
Expiry Date
Dec 13, 2025
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About this record

Access comprehensive regulatory information for "Mekewei" microporous membrane oxygenator with venous hard shell blood storage tank in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5054232b45c9079401931f0be5048cc0 and manufactured by Maquet Cardiopulmonary AG; MAQUET Cardiopulmonary Medikal Teknik San. Twitch. Ltd. Sti. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including MAQUET Cardiopulmonary Medikal Teknik San. Twitch. Ltd. Sti;; Maquet Cardiopulmonary GmbH, Maquet Cardiopulmonary AG; MAQUET Cardiopulmonary Medikal Teknik San. Twitch. Ltd. Sti, and 3 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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