Ketostix®
by Ascensia Diabetes Care Holdings AG 3 variants
Ref 746809Model KSTIX-U-XXXXYY
Ketostix® (746809) is a Class C device made by Ascensia Diabetes Care Holdings AG, registered in EUDAMED on 22 Sep 2026 (Basic UDI-DI 15016003KSTIXUBG8), active as of 7 Nov 2026.
Active
CE IVDR
Valid until
7 Jul 2030
FDA recalls
Not applicable
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/IVDR | Number15016003KSTIXUBG8 15016003288606 | Date22 Sep 2026 | StatusActive |
Official records
- EUDAMED public site 15016003KSTIXUBG8
Certificates
- IVDR 785590 Active
Technical documentation EU IVDR
- Certifier
- BSI Group The Netherlands B.V. 2797
- Issued
- 8 Jul 2025
- Expires
- 7 Jul 2030
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/IVDR Active
Specification
- Device name
- Ketostix Reagent Strips
- Model / reference
- KSTIX-U-XXXXYY, 746809
- Primary DI / UDI-DI
- 15016003288606
- Basic UDI-DI
- 15016003KSTIXUBG8
- Unit of use DI
- 25016003288603
- EMDN code
- W0101060201 Urine single test strips (incl. tablets)
- Device class
- Class C
- EU registration type
- Standard device
- EU market of registration
- Norway
Manufacturer details
- EUDAMED SRN
- CH-MF-000034124
- Authorised representative
- Ascensia Diabetes Care Italy Srl IT-AR-000025584
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