EUDAMED device
PERFLUORON
EUDAMED device 00380659001024 · Alcon Laboratories, Inc.
Key facts
| Primary DI | 00380659001024 |
|---|---|
| Trade name | PERFLUORON |
| Device name | Surgical PERFLUORON Kit |
| Reference or catalog number | 0090010019 |
| Manufacturer | Alcon Laboratories, Inc. |
| Manufacturer SRN | US-PR-000037951 |
| Risk class | Class IIa |
| EMDN code | Q02030205 |
| EMDN description | OPHTHALMIC SURGERY, PERFLUOROCARBONS PURE AND COMBINED WITH OTHER SUBSTANCES |
| Legislation | mdr |
| Implantable | No |
| Sterile | No |
| Single use | No |
| Status date | Jun 20, 2025 |
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: