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.
No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.
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 |