Taiwan FDA registration c5a898279fdda9973b64bd8d0a321cca
"Kabi" blood bag tube sealer (unsterilized)
TW: “卡比” 血袋管封口機 (未滅菌)
Taiwan·Risk Class 1·Fresenius Kabi AG; Fresenius HemoCare GmbH·Registered Oct 21, 2013 – Oct 21, 2028ActiveRegistration details
- Analysis ID
- c5a898279fdda9973b64bd8d0a321cca
- Customs Code
- DHA09401351603
Company information
- Manufacturer
- Fresenius Kabi AG; Fresenius HemoCare GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- FRESENIUS KABI TAIWAN LIMITED
Product details
- Intended Use
- Limited to the classification and grading management measures for medical equipment "Heating and Sealing Equipment (B.9750)" first level identification range.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9750 Heat-sealing equipment
- Import Information
- import
Dates and status
- Registration Date
- Oct 21, 2013
- Expiry Date
- Oct 21, 2028
About this record
Access comprehensive regulatory information for "Kabi" blood bag tube sealer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c5a898279fdda9973b64bd8d0a321cca and manufactured by Fresenius Kabi AG; Fresenius HemoCare GmbH. The authorized representative in Taiwan is FRESENIUS KABI TAIWAN LIMITED.
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