mdd Company GmbH
CH-MF-000009532 · Switzerland · Obernau
mdd Company GmbH is registered in the European database on medical devices as a manufacturer, with 120 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 106 |
|---|---|
| Class IIb | 14 |
Most frequent device types declared: Air Water Channel Cleaning Valve, Biopsy Valve, Bite Block, Cleaning Tube, Distal Protection Cleaning Sponge.
Authorised representative in the Union: Prolinx GmbH.
Devices declared under this manufacturer
- Biopsy Valve
- Bite Block
- Cleaning Brush
- Cleaning Valve
- Collector One
- Endoscope Protection Sponge
- HMC 0
- HMC 9
- HMC E
- HMC Enzyme
- HMC NF
- KIREIFLOW
Showing 12 of 120 declared devices.
Catalogue references include BV-FX-100, BV-PX-100, DCBS-08-10-15-230, DCBS-23-20-05-180, DCBS-23-20-05-230, DCBS-SET-23-20-05-240.
European nomenclature codes declared: V070101, G030804, G0380, D050103, A99, G0399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 120 |
| Country of registration | Switzerland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 120 |
|---|---|
| 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. mdd Company GmbH was not found in either the U.S. or the Canadian register.