Taiwan FDA registration 5e571e267b7ce7de693b7af3febb4c93
"Fresenius" blood cell separator cannula set
TW: “費森尤斯”血液細胞分離器套管組
Taiwan·Risk Class 2·FRESENIUS KABI AG;; FRESENIUS HEMOCARE NETHERLANDS B.V.·Registered Oct 27, 2008 – Oct 27, 2013CancelledRegistration details
- Analysis ID
- 5e571e267b7ce7de693b7af3febb4c93
- Customs Code
- DHA00601929800
Company information
- Manufacturer Country
- Germany;;Netherlands
- Authorized Representative
- Fresenius Kabi, Taiwan Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9100 Containers for the collection and disposal of blood and blood components
- Import Information
- import
Dates and status
- Registration Date
- Oct 27, 2008
- Expiry Date
- Oct 27, 2013
- Cancellation Date
- Apr 09, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Fresenius" blood cell separator cannula set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5e571e267b7ce7de693b7af3febb4c93 and manufactured by FRESENIUS KABI AG;; FRESENIUS HEMOCARE NETHERLANDS B.V.. The authorized representative in Taiwan is Fresenius Kabi, Taiwan Co., Ltd.
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