Taiwan FDA registration 5e111ffa3b5b871bbe7d9df05396a73d
"Kabi" Agelie's patient-controlled infusion helper
TW: “卡比”艾捷莉病患自控式輸液幫浦
Taiwan·Risk Class 2·Fresenius Vial S.A.S.;; Fresenius Kabi AG·Registered Aug 26, 2020 – Aug 26, 2025ExpiredRegistration details
- Analysis ID
- 5e111ffa3b5b871bbe7d9df05396a73d
- Customs Code
- DHA05603390200
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
- Aug 26, 2020
- Expiry Date
- Aug 26, 2025
About this record
Access comprehensive regulatory information for "Kabi" Agelie's patient-controlled infusion helper in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5e111ffa3b5b871bbe7d9df05396a73d 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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