UpHill Route
by Uphill S.A.
Ref UpHill Route
Active
CE MDR
Valid until
23 Jan 2030
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number56001398890DSSW9 05600139889009 | Date10 Mar 2026 | StatusActive |
Certificates
- 28620203207 Active
Quality management system EU MDR
- Certifier
- Intertek Medical Notified Body AB 2862
- Issued
- 24 Jan 2025
- Expires
- 23 Jan 2030
- 28620203207 Active
Quality management system EU MDR
- Certifier
- Intertek Medical Notified Body AB 2862
- Issued
- 24 Jan 2025
- Expires
- 23 Jan 2030
- Reason
- Add device or group
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / Reference
- UpHill Route
- Primary DI / UDI-DI
- 05600139889009
- Basic UDI-DI
- 56001398890DSSW9
- Direct Marketing DI
- 05600139889009
- EMDN Code
- V92 Medical device software - not included in other classes
- Device Class
- Class IIa
- Special Device Type
- Software
- EU market of registration
- Portugal
Manufacturer details
- EUDAMED SRN
- PT-MF-000021496
Properties
Other properties (13)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No