Taiwan FDA registration 67b70d80dd2f91b7dac1756763745065
"Deutschland" 5th generation automatic plasma pressure platen system
TW: “德意志”第五代自動血漿壓板系統
Taiwan·Risk Class 2·FRESENIUS KABI AG;; SANMINA-SCI·Registered Mar 06, 2012 – Mar 06, 2022CancelledRegistration details
- Analysis ID
- 67b70d80dd2f91b7dac1756763745065
- Customs Code
- DHA00602329608
Company information
- Manufacturer
- FRESENIUS KABI AG;; SANMINA-SCI
- Manufacturer Country
- Sweden;;Germany
- Authorized Representative
- FRESENIUS KABI TAIWAN LIMITED
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.0002 Blood Component Extraction Apparatus
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Mar 06, 2012
- Expiry Date
- Mar 06, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Deutschland" 5th generation automatic plasma pressure platen system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 67b70d80dd2f91b7dac1756763745065 and manufactured by FRESENIUS KABI AG;; SANMINA-SCI. The authorized representative in Taiwan is FRESENIUS KABI TAIWAN LIMITED.
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