Taiwan FDA registration dd98e9d39296ba3ef99323e4e9eda6e2
"Kabi" Jetley Infusion Pump Accessory
TW: “卡比”艾捷莉輸液幫浦配件
Taiwan·Risk Class 2·Fresenius Vial S.A.S.;; Fresenius Kabi AG·Registered Apr 19, 2016 – Apr 19, 2021CancelledRegistration details
- Analysis ID
- dd98e9d39296ba3ef99323e4e9eda6e2
- Customs Code
- DHA05602837904
Company information
- Manufacturer
- Fresenius Vial S.A.S.;; Fresenius Kabi AG
- Manufacturer Country
- France;;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)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5725 Infusion 幫浦
- Import Information
- import
Dates and status
- Registration Date
- Apr 19, 2016
- Expiry Date
- Apr 19, 2021
- Cancellation Date
- Aug 28, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kabi" Jetley Infusion Pump Accessory in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dd98e9d39296ba3ef99323e4e9eda6e2 and manufactured by Fresenius Vial S.A.S.;; Fresenius Kabi AG. The authorized representative in Taiwan is FRESENIUS KABI TAIWAN LIMITED.
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