KliniBand Kft.
HU-MF-000047539 · Hungary · Hajdúböszörmény
KliniBand Kft. is registered in the European database on medical devices as a manufacturer, with 462 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 462 |
|---|
Devices declared under this manufacturer
- Höga-Haft-Color 6 cm x 4 m grün kohäsive, elastische Fixierbinde
- Höga-Haft-Color 6 cm x 4 m rot kohäsive, elastische Fixierbinde
- Höga-Haft-Color 8 cm x 4 m rot kohäsive, elastische Fixierbinde
- Klini Crepp Haft 10cmx4m brown EZP 1 pc
- Klini Crepp Stretch Haft 8cmx4m brown
- Klini Crepp Stretch Haft 8cmx4m white
- Klini Flex Haft 8cmx20m brown EZP 1 pc
- Klini Flex Haft 8cmx4m brown
- Klini Flex Light 10cmx4m brown KLP
- Klini Flex Light 6cmx4m brown
- Klini Flex Stretch 12cmx4m white KLP
- Klini Flex Stretch Haft 4cmx4m brown
Showing 12 of 462 declared devices.
Catalogue references include 10933106, 10933135, 1100512, KB00410120040, KB10120100040, KB10320080040.
European nomenclature codes declared: M0303010201, M0303010101, M0304010102, M0304010202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 462 |
| Country of registration | Hungary |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 462 |
|---|---|
| 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. KliniBand Kft. was not found in either the U.S. or the Canadian register.