EUDAMED device
Secondary Antisera
EUDAMED device 00810108717058 · ScyTek Laboratories Inc.
Key facts
| Primary DI | 00810108717058 |
|---|---|
| Device name | Secondary Antisera |
| Reference or catalog number | PAM999 |
| Manufacturer | ScyTek Laboratories Inc. |
| Manufacturer SRN | US-MF-000023816 |
| Risk class | Class A |
| EMDN code | W01030710 |
| EMDN description | SECONDARY ANTISERA FOR IMMUNOHISTOLOGY |
| Legislation | ivdr |
| Implantable | No |
| Sterile | No |
| Single use | No |
| Status date | Dec 7, 2022 |
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: