Jolife AB
SE-MF-000002091 · Sweden · Lund
Jolife AB is registered in the European database on medical devices as a manufacturer, with 13 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIb | 13 |
|---|
Most frequent device types declared: 08858250000696SQ.
Among these devices, 13 are declared active.
Devices declared under this manufacturer
- LUCAS 3 Chest Compression System
Showing 12 of 13 declared devices.
Catalogue references include 99576-000064, 99576-000069, 99576-000070, 99576-000072, 99576-000073, 99576-000074.
European nomenclature codes declared: Z120304.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | JOLIFE AB (SE) · FDA 3005445717 |
| Devices in EUDAMED | 13 |
| Country of registration | Sweden |
Device-level evidence
| Devices with a numeric GTIN | 13 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | JOLIFE AB |
What it holds in Canada
| Licences on record | 2 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 2 |
| First licensed | 2009-04-03 |
Licence types: System (2).
Licensed under: LUCAS 2 CHEST COMPRESSION SYSTEM, LUCAS 3 CHEST COMPRESSION SYSTEM.
North American profile: Both markets. Jolife AB is registered in both the United States and Canada.