"Meikewei" infant microporous membrane oxygenator
Taiwan·Risk Class 2·Maquet Cardiopulmonary GmbH;; MAQUET Cardiopulmonary GmbH·Registered May 06, 2011 – May 06, 2026Cancelled- Analysis ID
- dc2a0b3982397c468d422f92ed343f62
- Customs Code
- DHA00602230201
- Manufacturer Country
- 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
- May 06, 2011
- Expiry Date
- May 06, 2026
- Cancellation Date
- Jun 27, 2023
- Status
- Logged out
- Reason
- 自請註銷
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Access comprehensive regulatory information for "Meikewei" infant microporous membrane oxygenator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dc2a0b3982397c468d422f92ed343f62 and manufactured by Maquet Cardiopulmonary GmbH;; 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 2 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.