Franz Kalff GmbH
DE-MF-000005326 · Germany · Euskirchen
Franz Kalff GmbH is registered in the European database on medical devices as a manufacturer, with 225 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 225 |
|---|
Devices declared under this manufacturer
- BANDAGES ELASTIC
- Bandages cohesive
- Dreiecktuch
- Elastic Bandages
- Elastic bandage
- Elastische Fixierbinde
- FINGER BANDAGE COHESIVE
- FIXIERBANDAGE KOHÄSIV
- Finger bandage - cohesive
- Heftpflaster
- Pflasterset, 14 teilig
- SPORTS TAPE
Showing 12 of 225 declared devices.
Catalogue references include 3753 LB, 3759 LV/LQ/LX, 3762 LI/LÖ/LY/LH/LN/LB, 3763 LD/LL/L9/LF, U07485, U07911.
European nomenclature codes declared: M050101, M0303010101, M04010199, M0303010201, M030402020101, M050202.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | FRANZ KALFF GMBH (DE) · FDA 3002801783 |
| Devices in EUDAMED | 225 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 225 |
|---|---|
| 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. Franz Kalff GmbH is registered in the United States but was not found in the Canadian register.