KERN LIEBERS Schwabmünchen GmbH
DE-MF-000010123 · Germany · Schwabmünchen
KERN LIEBERS Schwabmünchen GmbH is registered in the European database on medical devices as a manufacturer, with 15 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 15 |
|---|
Most frequent device types declared: MediLance, medi Lance, mediLance.
Among these devices, 15 are declared sterile.
Devices declared under this manufacturer
- ALK Lancet
- AMEFA medimex Blutlanzetten
- Allergy Therapeutics Lancet
- Assistent Blutlanzetten
- HAL Allergy Prick lancets
- HHH Allergielanzette
- HHH Blutlanzette
- Immuntek Allergy lancets
- Leti-Lancetas
- Roxall Prick Lanzetten
- Stallergenes Prick Lancets
- allergopharma Prick-Test-Lancet
Showing 12 of 15 declared devices.
Catalogue references include A01F005, Schlüsselnummer 301, Schlüsselnummer 621, Schlüsselnummer 625, Schlüsselnummer 701, Schlüsselnummer 760.
European nomenclature codes declared: W01020299, V010402.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 15 |
| 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 | 15 |
|---|---|
| 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. KERN LIEBERS Schwabmünchen GmbH was not found in either the U.S. or the Canadian register.