EUDAMED device
MANUAL RETRACTION KIT
EUDAMED device 00763000228699 · Medtronic, Inc.
Key facts
| Primary DI | 00763000228699 |
|---|---|
| Device name | MANUAL RETRACTION KIT |
| Reference or catalog number | 20MRK |
| Manufacturer | Medtronic, Inc. |
| Manufacturer SRN | US-MF-000019977 |
| Risk class | Class I |
| EMDN code | C0280 |
| EMDN description | ARRYTHMOLOGY DEVICES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES |
| Legislation | mdr |
| Implantable | No |
| Sterile | Yes |
| Single use | Yes |
| Status date | Feb 9, 2026 |
At a glance
- Yes 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: