Taiwan FDA registration 7088790e7ed86ea4f1ece8a6686f8f5e
"Kirby" Knoss High Level Anesthesia Depth Monitor
TW: “卡比”克諾斯高階麻醉深度監測儀
Taiwan·Risk Class 2·Fresenius Vial S.A.S.;; Fresenius Kabi AG·Registered May 31, 2024 – May 31, 2029ActiveRegistration details
- Analysis ID
- 7088790e7ed86ea4f1ece8a6686f8f5e
- Customs Code
- DHA05603718900
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
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.1400 Brain Wave Scanner
- Import Information
- import
Dates and status
- Registration Date
- May 31, 2024
- Expiry Date
- May 31, 2029
About this record
Access comprehensive regulatory information for "Kirby" Knoss High Level Anesthesia Depth Monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7088790e7ed86ea4f1ece8a6686f8f5e 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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