Ludwig Artzt GmbH
DE-MF-000012141 · Germany · Dornburg
Ludwig Artzt GmbH is registered in the European database on medical devices as a manufacturer, with 54 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 54 |
|---|
Most frequent device types declared: Balance Flooring, Instrument Assisted Massage, Kinesiology Tape, Resistance Band, Sports Tape.
Devices declared under this manufacturer
- ARTZT thepro Cranibas professional
- ARTZT thepro Fazer 1
- ARTZT thepro Fazer 2
- ARTZT thepro Fazer 4
- ARTZT thepro Kinesiologisches Tape 2er-Set schwarz
- ARTZT thepro Kinesiologisches Tape 2er-Set schwarz-blau
- ARTZT thepro Kinesiologisches Tape 5 m blau
- ARTZT thepro Kinesiologisches Tape 5 m pink
- ARTZT vitality Stabilitätstrainer medium/blau
- TheraBand Travel blau
- TheraBand Übungsband 2,5 m grün
- TheraBand Übungsband 2,5 m schwarz
Showing 12 of 54 declared devices.
Catalogue references include 27927, 27929, 27929R, LA-5011, LA-7013, LA-7021.
European nomenclature codes declared: Z120602, M050201, M050202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 54 |
| 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 | 54 |
|---|---|
| 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. Ludwig Artzt GmbH was not found in either the U.S. or the Canadian register.