Localite GmbH
DE-MF-000005419 · Germany · Bonn
Localite GmbH is registered in the European database on medical devices as a manufacturer, with 66 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 66 |
|---|
Most frequent device types declared: Fußschalter, Pointer, TMS Navigator Software 3, Tracker.
Among these devices, 6 are declared active.
Devices declared under this manufacturer
- Kalibirerplatte
- Klebbare Basis für Tracker
- Klebepads, rund (250 St.)
- Kopftrackeraufsatz MR
- MR Kameragestell
- MR-Fußschalter, 3 Taster
- Pointer ST
- TMS Navigator SW MR-Less
- Trackeraufsatz MR, Geo. 1
- Trackeraufsatz MR, Geo. 2
- Trackeraufsatz, Geo. 1
- Trackerring, 25 mm
Showing 12 of 66 declared devices.
Catalogue references include 001223, 002006, 003221, 010206, 010218, 014221.
European nomenclature codes declared: V9099, V92.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | LOCALITE GMBH (DE) · FDA 3017603615 |
| Devices in EUDAMED | 66 |
| Country of registration | Germany |
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: United States only. Localite GmbH is registered in the United States but was not found in the Canadian register.