Laboratorium Dr. Deppe GmbH
DE-MF-000005103 · Germany · Kempen
Laboratorium Dr. Deppe GmbH is registered in the European database on medical devices as a manufacturer, with 335 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 291 |
|---|---|
| Class IIb | 44 |
Devices declared under this manufacturer
- ARNOMED DesiQuick
- CAMED Desinfektionsmegatücher
- Enzym Med Wipes
- MaiMed MyClean B
- MaiMed MyClean IN
- Medizid Alpha+
- Micro Clean ECO XXL BioWipes
- Micro Clean GT XXL
- Micro Clean PRO XXL Wipes
- Spray In QF
- Spray Off Bio Wipes
- Spray Off Wipes
Showing 12 of 335 declared devices.
Catalogue references include 600614, 600951, 601414, 601787, 601842, 601981.
European nomenclature codes declared: D99, D0701, D0901, D0801, D0799, D0199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 335 |
| 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 | 335 |
|---|---|
| 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. Laboratorium Dr. Deppe GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
44911220522 | issued | 2029-04-10 |