Kfbio
by Ningbo Konfoong Bioinformation Tech Co., Ltd. 15 variants
Ref 0568Model KF-SLBF-22S
Kfbio (0568) is an in vitro diagnostic device (EU IVDR Class A; EMDN category IVD general use consumable devices) made by Ningbo Konfoong Bioinformation Tech Co., Ltd., registered in EUDAMED on 22 Sep 2026 (Basic UDI-DI 697533071KFSLBF22SNA), active as of 25 Oct 2026.
Active
CE IVDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/IVDR | Number697533071KFSLBF22SNA 06975330710568 | Date22 Sep 2026 | StatusActive |
Official records
- EUDAMED public site 697533071KFSLBF22SNA
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/IVDR Active
Specification
- Device name
- Buffer Solution
- Model / reference
- KF-SLBF-22S, 0568
- Primary DI / UDI-DI
- 06975330710568
- Basic UDI-DI
- 697533071KFSLBF22SNA
- EMDN code
- W0599 IVD general use consumable devices - other
- Device class
- Class A
- EU registration type
- Standard device
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- CN-MF-000030466
- Authorised representative
- Share info GmbH DE-AR-000005132
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