WERUNIA GmbH
DE-MF-000007299 · Germany · Kreischa
WERUNIA GmbH is registered in the European database on medical devices as a manufacturer, with 135 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 135 |
|---|
Devices declared under this manufacturer
- 10er Fingerverband 12 x 2 cm
- 10er Kinder-Pflaster \
- PL Haftbandagen 10 cm x 2.8m Colour Blau TD
- PL Haftbandagen 10 cm x 2.8m Design Tarn TD
- PL Haftbandagen 2.5cm x 2.8m Design Zebra TD
- Pflaster sensitiv Kids KIK
- Pflasterbriefchen - hypoallergen blau
- Pflasterbriefchen Dinosaurier
- Pflasterbriefchen Living Puppets
- Pflasterbriefchen Space
- Selbsthaftende Bandage 2,5 cm x 4,5 m waldgrün
- Selbsthaftende Bandage 10 cm x 2,8 m
Showing 12 of 135 declared devices.
Catalogue references include 10013, 10024, 10122, 10134, 12010, 12020.
European nomenclature codes declared: M0599, M0303010201, M04010299, M020205, M9001, M030402010103.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 135 |
| 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 | 135 |
|---|---|
| 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. WERUNIA GmbH was not found in either the U.S. or the Canadian register.