medmix Deutschland GmbH
DE-MF-000011201 · Germany · Kiel
medmix Deutschland GmbH is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 5 |
|---|
Among these devices, 5 are declared sterile.
Devices declared under this manufacturer
- transcodent Hypodermic Needles
- transcodent Irrigation Needles
- transcodent Painless Steel
- transcodent Paste Needles
- transcodent Suction Needles
Catalogue references include 162020, 163689, 164499, 164524, 164913.
European nomenclature codes declared: Q010599, A0101010102, Q010506.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | medmix Deutschland GmbH (DE) · FDA 3007113445 |
| Devices in EUDAMED | 5 |
| Country of registration | Germany |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | MEDMIX DEUTSCHLAND GMBH |
North American profile: Both markets. medmix Deutschland GmbH is registered in both the United States and Canada.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
6265GB448260219 | supplemented | 2030-03-02 |