Apaloo GmbH
DE-MF-000016970 · Germany · Talheim
Apaloo GmbH is registered in the European database on medical devices as a manufacturer, with 41 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 41 |
|---|
Most frequent device types declared: 10101, 10110, 10110-S, Kinesiologie Tape Classic Darkblue, Kinesiologie Tape Classic Yellow.
Devices declared under this manufacturer
- E.CHi
- Insect Protect Pansements Après Piqures
- Kintex
- Moskinto
- Pro Touch
Showing 12 of 41 declared devices.
Catalogue references include 10101-2, 10109, 10110, 10130, 10180, 11150.
European nomenclature codes declared: H900299, M0599.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 41 |
| 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 | 41 |
|---|---|
| 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. Apaloo GmbH was not found in either the U.S. or the Canadian register.