Taiwan FDA registration 5df12c75b3dcd251a494bf932d46652d
"Kabi" Ajili infusion pump
TW: “卡比”艾捷莉輸液幫浦
Taiwan·Risk Class 2·Fresenius Vial S.A.S.;; Fresenius Kabi AG·Registered May 16, 2018 – May 16, 2028ActiveRegistration details
- Analysis ID
- 5df12c75b3dcd251a494bf932d46652d
- Customs Code
- DHA05603089501
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
- May 16, 2018
- Expiry Date
- May 16, 2028
About this record
Access comprehensive regulatory information for "Kabi" Ajili infusion pump in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5df12c75b3dcd251a494bf932d46652d 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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