Scholz Medical GmbH
DE-MF-000008955 · Germany · Bruckmuehl
Scholz Medical GmbH is registered in the European database on medical devices as a manufacturer, with 226 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 226 |
|---|
Most frequent device types declared: 426052621TABC01WZ, 426052621TABD01X6, Pinzetten, Schere, Scheren.
Among these devices, 226 are declared sterile.
Devices declared under this manufacturer
- Anatomische Pinzette, Standard, 145 mm
- Chirurgische Schere spitz/spitz gebogen 145mm
- Knopfkanüle 1,2 x 80 mm gebogen B, LL
- Knopfkanüle 1,6 x 100 mm gerade A, LL
- Ligaturschere spitz/spitz gebogen 115 mm
- Mayo-Hegar Nadelhalter, 120 mm
- Saugkanüle, Fergusson, GL: 215mm, AL: 130mm, AD: 2,0mm
- Saugkanüle, Fergusson, GL: 215mm, AL: 130mm, AD: 5,0mm
- Scharfer Löffel, Doppellöffel, 210 mm
- Schlauchklemme, Kunststoff, grün, 120 mm
- Spekulum nach Kilian, 30 mm Schaft
- Splitterpinzette gerade 110 mm
Showing 12 of 226 declared devices.
Catalogue references include 326422, SIGF3650, SIOK0811, TABC1011, TABC3433, TABC4444.
European nomenclature codes declared: V901699.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 226 |
| 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 | 226 |
|---|---|
| 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. Scholz Medical GmbH was not found in either the U.S. or the Canadian register.