cortiQ PRO
by g.tec medical engineering GmbH 3 variants
Ref 8073
cortiQ PRO (8073) is a medical device (EU MDR Class IIb; EMDN category cerebral mapping systems) made by g.tec medical engineering GmbH, registered in EUDAMED on 4 Apr 2025 (Basic UDI-DI ++EBCI8060MA), active as of 25 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number++EBCI8060MA 8073 | Date4 Apr 2025 | StatusActive |
Official records
- EUDAMED public site ++EBCI8060MA
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- cortiQ PRO
- Model / reference
- 8073
- Primary DI / UDI-DI
- 8073
- Basic UDI-DI
- ++EBCI8060MA
- Direct marketing DI
- 8073
- EMDN code
- Z12101104 Cerebral mapping systems
- Device class
- Class IIb
- EU registration type
- Standard device
- EU market of registration
- Austria
Manufacturer details
- EUDAMED SRN
- AT-MF-000004562
From the manufacturer
Manufacturer's product page: cortiQ PRO 2.0Fast Cortical Mapping for Enhanced Surgical Outcomes in Epilepsy and Brain Tumors START CONFIGURATOR ›
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