femtos GmbH
DE-MF-000005499 · Germany · Bochum
femtos GmbH is registered in the European database on medical devices as a manufacturer, with 17 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 17 |
|---|
Most frequent device types declared: PEGASUS-350-15, PEGASUS-350-20, PEGASUS-350-20-HPC, PEGASUS-350-25-HPC, PEGASUS-350-30.
Among these devices, 17 are declared sterile, 16 implantable.
Devices declared under this manufacturer
- pEGASUS HPC Stent System
- pEGASUS Stent System
- pRELAX - Vasospasm Treatment Device
Showing 12 of 17 declared devices.
Catalogue references include PEGASUS-350-15, PEGASUS-350-20-HPC, PEGASUS-350-25-HPC, PEGASUS-350-30, PEGASUS-450-15-HPC, PEGASUS-450-20.
European nomenclature codes declared: P0704020202, P070402020102, C0104040299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 17 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 17 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. femtos GmbH was not found in either the U.S. or the Canadian register.