"Meikewei" infant microporous membrane oxygenator with venous hard shell blood storage tank
Taiwan·Risk Class 2·MAQUET Cardiopulmonary Medikal Teknik San. Twitch. Ltd. Sti;; MAQUET CARDIOPULMONARY AG·Registered Sep 30, 2011 – Sep 30, 2026Active- Analysis ID
- a014ca1ea9d3a4eea18bc16d159bddfa
- Customs Code
- DHA00602282800
- Manufacturer Country
- Türkiye;;Germany
- Authorized Representative
- GETINGE GROUP TAIWAN CO., LTD.
- 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.4350 Cardiopulmonary vascular bypass and oxygen apparatus
- Import Information
- import
- Registration Date
- Sep 30, 2011
- Expiry Date
- Sep 30, 2026
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Access comprehensive regulatory information for "Meikewei" infant 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 a014ca1ea9d3a4eea18bc16d159bddfa 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 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.