Álvarez Redondo, S.A.
ES-MF-000000560 · Spain · MADRID
Álvarez Redondo, S.A. is registered in the European database on medical devices as a manufacturer, with 35 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: CE 110IVD, CE 146IVD, CE 156IVD, CE 202IVD, CE 223IVD.
Devices declared under this manufacturer
- Biocen 22 R
- Bioprocen 22 R
- Consul 22
- Consul 22R
- Cyto 1
- Digicen 21
- Digicen 21R
- Digicen 22
- Digtor 22
- MICROCEN 24
- Magnus
- Magnus 22
Showing 12 of 35 declared devices.
Catalogue references include CE 113IVD, CE 148IVD, CE 224IVD, CE 227IVD, CE 230IVD, CE 232IVD.
European nomenclature codes declared: W02069003, W02069005, W02069004.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 35 |
| Country of registration | Spain |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 35 |
|---|---|
| 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. Álvarez Redondo, S.A. was not found in either the U.S. or the Canadian register.