CANNORDIC A/S
DK-MF-000003852 · Denmark · København Ø
CANNORDIC A/S is registered in the European database on medical devices as a manufacturer, with 14 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 14 |
|---|
Most frequent device types declared: MDARTG20, MDNASG21, MDNASS22, MDPAIP21, MDPSOG20.
Devices declared under this manufacturer
- Algyl CBD náplast na bolest
- Biobloom CBD Pain Patch
- CALMADOL MDR Cerotto per Dolori
- CANNASEN Pain Patch
- CANNASEN Psoriasis Gel
- CANNASEN® Nasal Night Spray
- CANNASEN® Nasal Protect Gel
- CANNASEN® Pain & Arthritis Gel
- CANNASEN® Pain Patch [EN]
- CANNASEN® Psoriasis Gel
- CANNASEN® Wound Gel
- Cannabidoc SCHMERZ PFLASTER [DE]
Showing 12 of 14 declared devices.
Catalogue references include 10252203174, AL-1120-605-07, CSNS-100101, HT-1220-624-06, PL-CSPP100301, PL-CSPP100303.
European nomenclature codes declared: M0599, M9002, M9001, M04040102, M04040501, Q030199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 14 |
| 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 | 14 |
|---|---|
| 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. CANNORDIC A/S was not found in either the U.S. or the Canadian register.