EUDAMED device
ECOR
EUDAMED device 00815203021390 · ElectroCore, Inc.
Key facts
| Primary DI | 00815203021390 |
|---|---|
| Trade name | ECOR |
| Device name | gammaCore Sapphire |
| Reference or catalog number | 12016-08594 |
| Model | gammaCore Sapphire SLC Refill Card Evaluation Kit |
| Manufacturer | ElectroCore, Inc. |
| Manufacturer SRN | US-MF-000036987 |
| Risk class | Class IIa |
| EMDN code | Z12101106 |
| EMDN description | NEUROLOGICAL STIMULATORS |
| Legislation | mdd |
| Implantable | No |
| Sterile | No |
| Single use | No |
| Status date | Oct 24, 2024 |
At a glance
- No Matching FDA GUDID record
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About EUDAMED devices
EUDAMED is the European Union's database of medical devices registered under the MDR and IVDR, including UDI-DIs, risk classes and EMDN nomenclature codes.
Source: European Commission, European Database on Medical Devices (EUDAMED) · Source date: