Taiwan FDA registration ba9066946a1dc167975289b2a2313f3f
"Deutschland" plasma platen (unsterilized)
TW: 〝德意志〞 血漿壓板 (未滅菌)
Taiwan·Risk Class 1·FRESENIUS KABI AG·Registered Mar 28, 2006 – Mar 28, 2016CancelledRegistration details
- Analysis ID
- ba9066946a1dc167975289b2a2313f3f
- Customs Code
- DHA04400323101
Company information
- Manufacturer
- FRESENIUS KABI AG
- Manufacturer Country
- Germany
- Authorized Representative
- Fresenius Kabi, Taiwan Co., Ltd
Product details
- Intended Use
- First, the blood components in whole blood are layered by centrifuge, and then separated into concentrated red blood cells, white blood cells, platelets, plasma and other blood components through a plasma pressure plate.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9050 Blood bank supply equipment
- Import Information
- import
Dates and status
- Registration Date
- Mar 28, 2006
- Expiry Date
- Mar 28, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Deutschland" plasma platen (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ba9066946a1dc167975289b2a2313f3f and manufactured by FRESENIUS KABI AG. The authorized representative in Taiwan is Fresenius Kabi, Taiwan Co., Ltd.
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