Navbit Sprint
by Navbit Pty Ltd EUDAMEDGUDID
Withdrawn
Ref HBS-00-001Model HBS-01-001
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-09369998068180 | Date19 Jul 2023 | StatusWithdrawn |
| United States | GUDID listing GUDID | Number09369998068180 | Date27 Apr 2021 | StatusWithdrawn |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
- European Union
- United States
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls on record, checked 24 Oct 2026.
Specification
- Trade Name
- Navbit Sprint EUDAMEDNavbit Sprint_Supine GUDID
- Generic Name
- Orthopaedic stereotactic surgery system
- Device Name
- Navbit Sprint Device, Supine Registration
- Model / Reference
- HBS-01-001, HBS-00-001
- Primary DI / UDI-DI
- 09369998068180
- Basic UDI-DI
- B-09369998068180
- FDA Product Code
- OLO
- EMDN Code
- Z12130401 Stereotactic orthopaedic surgery systems
- GMDN Term
- Orthopaedic stereotactic surgery system
- Device Class
- Class IIa EUDAMEDClass II GUDID
- Regulation Number
- 882.4560
- Market of Registration
- Northern Ireland
- Commercial Distribution
- Not in Commercial Distribution
- MRI Safety
- MR Unsafe
- Size
- Length — 3 Inch
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class IIa | Class II |
Manufacturer details
- EUDAMED SRN
- AU-MF-000016920
- Authorised representative
- Emergo Europe B.V. NL-AR-000000116
Other devices from Navbit Pty Ltd
Properties
Other properties (14)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Administering Medicine: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No