Taiwan FDA registration 6b1b09dac3f3e60457ee4c2028ace9ef
Plum plasma component separator
TW: 英弗梅血漿成分分離器
Taiwan·Risk Class 3·Membrane GmbH;;Infomed S.A.·Registered Dec 10, 2015 – Dec 10, 2020CancelledRegistration details
- Analysis ID
- 6b1b09dac3f3e60457ee4c2028ace9ef
- Customs Code
- DHA05602799202
Company information
- Manufacturer
- Membrane GmbH;;Infomed S.A.
- Manufacturer Country
- Germany;;Switzerland
- Authorized Representative
- HEMOSCIEN CORPORATION
Product details
- Intended Use
- This product is used to separate substances from plasma in the blood.
- Product Type (Level 1)
- H Gastroenterology and urology
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Dec 10, 2015
- Expiry Date
- Dec 10, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Plum plasma component separator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 6b1b09dac3f3e60457ee4c2028ace9ef and manufactured by Membrane GmbH;;Infomed S.A.. The authorized representative in Taiwan is HEMOSCIEN CORPORATION.
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices