MEIKO Maschinenbau GmbH & Co. KG
DE-MF-000005536 · Germany · Offenburg
MEIKO Maschinenbau GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 11 |
|---|
Among these devices, 11 are declared active.
Devices declared under this manufacturer
- MEIKO TOPIC 10
- MEIKO TOPIC 20
- MEIKO TOPIC 40
- MEIKO TopLine 10
- MEIKO TopLine 10 Type M2
- MEIKO TopLine 20
- MEIKO TopLine 20 Type M2
- MEIKO TopLine 30
- MEIKO TopLine 30 Type M2
- MEIKO TopLine 40
- MEIKO TopLine 40 Type M2
European nomenclature codes declared: Z12011301.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | MEIKO MASCHINENBAU GMBH & CO. KG (DE) · FDA 3006542588 |
| Devices in EUDAMED | 11 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 11 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | MEIKO MASCHINENBAU GMBH & CO. KG |
What it holds in Canada
| Licences on record | 3 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 3 |
| First licensed | 2006-05-26 |
Licence types: Device Family (2), Device Group Family (1).
Licensed under: MEIKO TOPLINE, MEIKO TOPIC, MEIKO TOPLINE TYPE M2.
North American profile: Both markets. MEIKO Maschinenbau GmbH & Co. KG is registered in both the United States and Canada.