DEWIMED Medizintechnik GmbH
DE-MF-000011317 · Germany · Tuttlingen
DEWIMED Medizintechnik GmbH is registered in the European database on medical devices as a manufacturer, with 317 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 317 |
|---|
Among these devices, 177 are declared reusable.
Devices declared under this manufacturer
- AGGRESSIVE FULL-RADIUS 4,2Ø MM, CURVED AUTOCLAVABLE, ARTHREX APS II, R
- DEWILUX 130 LED LC,130.000lx,4.900K,Ra96 Lightfield d10 (1m): 150-280m
- DEWILUX 130/130 LED DOUBLE OPERATION LIGHT
- DEWILUX 160/130 LED WITH CAMERA AND MONITOR (WITHOUT 3RD ARM)
- DEWILUX 160/130 LED WITH CAMERA AND MONITOR AND 3RD ARM
- DEWILUX 160/160 LED DOUBLE CEILING LIGHT
- SET 160/130 with Central Axis and 1x DEWILUX 130 LED / 1x DEWILUX 160
- SET DEWILUX 130 LED lamp, 130 KLUX consisiting of:
- SET DEWILUX 160 LED lamp, 160 KLUX consisting of:
- SET Double Lights with Central Axis and 2 x DEWILUX 130 LED LC, consis
- SET Mobile Light with DEWILUX LED 130 consisting of:
Showing 12 of 317 declared devices.
Catalogue references include 15-60340S, 15-65320S, 15-65580S, 15-66431, 15-71310, 15-71540.
European nomenclature codes declared: L1999, K030203, Z129004, K030204, Z1202110201.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | DEWIMED MEDIZINTECHNIK GMBH (DE) · FDA 3000286616 |
| Devices in EUDAMED | 317 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 317 |
|---|---|
| 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: United States only. DEWIMED Medizintechnik GmbH is registered in the United States but was not found in the Canadian register.