Qufora A/S
DK-MF-000007943 · Denmark · Alleroed
Qufora A/S is registered in the European database on medical devices as a manufacturer, with 53 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 53 |
|---|
Most frequent device types declared: Bed, Flow, MiniGo.
Devices declared under this manufacturer
- Qufora IrriSedo Klick Accessory Set ML
- Qufora IrriSedo MiniGo Flex Teaching set UK
- Qufora IrriSedo MiniGo Flex base set ML
- Qufora IrriSedo MiniGo Flex basisset DE
- Qufora IrriSedo MiniGo Flex small ML
- Qufora IrriSedo MiniGo Flex small teaching set UK
- Qufora IrriSedo MiniGo Flex startsæt
- Qufora IrriSedo MiniGo Flex teaching set ML
- Qufora IrriSedo MiniGo Small NL
- Qufora IrriSedo MiniGo Small Teaching set ML
- Qufora IrriSedo MiniGo Teaching set SE
- Qufora IrriSedo MiniGo accessoire set NL
Showing 12 of 53 declared devices.
Catalogue references include 51101-001, 57002-005, 57004-015, 57006-030, 57011-005, 57011-105.
European nomenclature codes declared: A03040299, A99,G99.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 53 |
| Country of registration | Denmark |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 53 |
|---|---|
| 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. Qufora A/S was not found in either the U.S. or the Canadian register.