Laboratoires PAUL HARTMANN S.à.r.l
FR-MF-000004029 · France · Sélestat cedex
Laboratoires PAUL HARTMANN S.à.r.l is registered in the European database on medical devices as a manufacturer, with 77 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 77 |
|---|
Most frequent device types declared: 1082, 1266, 1271, 3406.
Among these devices, 9 are declared sterile.
Devices declared under this manufacturer
- Foliodress® Suit
- Foliodress® Suit Protect
- Stérilux® ES
Showing 12 of 77 declared devices.
Catalogue references include 205028, 241326, 50755, 992516, 992540, 992549.
European nomenclature codes declared: T0299, M020199, V0199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 77 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 77 |
|---|---|
| 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. Laboratoires PAUL HARTMANN S.à.r.l was not found in either the U.S. or the Canadian register.