Taiwan FDA registration 261eb7931c4e3dab7636362e96256ce1
''Kabi" Tube Sealer (Non-Sterile)
TW: "卡比" 血袋封口機 (未滅菌)
Taiwan·Risk Class 1·MD·FRESENIUS KABI AG·Registered Jul 29, 2020 – Jul 29, 2025ExpiredRegistration details
- Analysis ID
- 261eb7931c4e3dab7636362e96256ce1
- License Form
- Ministry of Health Medical Device Import No. 021799
- Customs Code
- DHA09402179901
Company information
- Manufacturer
- FRESENIUS KABI AG
- Manufacturer Country
- Germany
- Authorized Representative
- FRESENIUS KABI TAIWAN LIMITED
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Heating and Sealing Equipment (B.9750)".
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B9750 Heat sealing equipment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 29, 2020
- Expiry Date
- Jul 29, 2025
About this record
Access comprehensive regulatory information for ''Kabi" Tube Sealer (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 261eb7931c4e3dab7636362e96256ce1 and manufactured by FRESENIUS KABI AG. The authorized representative in Taiwan is FRESENIUS KABI TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices