Log10 B.V.
NL-MF-000000057 · Netherlands · Eindhoven
Log10 B.V. is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 4 |
|---|---|
| Class IIb | 1 |
Most frequent device types declared: 50101.
Among these devices, 1 are declared sterile, 1 active.
Devices declared under this manufacturer
- Summox One System
- Summox Smart Container for General Instruments - full-sized
- Summox Smart Container for General Instruments - half-sized
- Summox Smart Container for Handpieces - full-sized
- Summox Smart Seal
Catalogue references include 50101, 60110, 60120, 60150, 70401.
European nomenclature codes declared: S010499, S0199, V0799, Z12011306.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| Country of registration | Netherlands |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 5 |
|---|---|
| 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. Log10 B.V. was not found in either the U.S. or the Canadian register.