EUDAMED device
Mark-Through GuideLines
EUDAMED device 00815137021121 · Beekley Corporation
Key facts
| Primary DI | 00815137021121 |
|---|---|
| Device name | Mark-Through GuideLines |
| Reference or catalog number | 219 |
| Model | 219 |
| Manufacturer | Beekley Corporation |
| Manufacturer SRN | US-MF-000007055 |
| Risk class | Class I |
| EMDN code | Z11030585 |
| EMDN description | RADIOLOGY INSTRUMENTS - CONSUMABLES |
| Legislation | mdr |
| Implantable | No |
| Sterile | No |
| Single use | Yes |
| Status date | Dec 19, 2024 |
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: