Laboratorios Cinfa, S.A.
ES-MF-000001574 · Spain · Huarte
Laboratorios Cinfa, S.A. is registered in the European database on medical devices as a manufacturer, with 330 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 330 |
|---|
Most frequent device types declared: ARMALASTIC MUÑEQUERA UNIVERSAL COMPRESSION TECH, FARMALASTIC CABESTRILLO BANDA UNIVERSAL ADVANCE TECH, FARMALASTIC CALCETÍN(A-D) COMPRESIÓN NORMAL, FARMALASTIC FAJA LUMBOABDOMINAL ABIERTA VELCRO®, FARMALASTIC FAJA LUMBOSACRA EXTRA.
Among these devices, 298 are declared reusable.
Devices declared under this manufacturer
- FARMALASTIC CABESTRILLO BANDA UNIVERSAL ADVANCE TECH Talla Única Color
- FARMALASTIC Calcetín (A-D) Compresión normal negro talla P
- FARMALASTIC FAJA ABDOMINAL MULTIBANDA MONOFILAMENTO Talla G Color Blan
- FARMALASTIC FAJA LUMBOABDOMINAL ABIERTA VELCRO® Talla P Color Beige
- FARMALASTIC FAJA LUMBOSACRA CLÁSICA Talla G Color Beige
- FARMALASTIC MEDIA CORTA PUNTERA CERRADA COMPRESIÓN FUERTE Color Beige
- FARMALASTIC MEDIAS TERAPÉUTICAS COMPRESIÓN LIGERA PANTY (EJECUTIVO MUJ
- FARMALASTIC MUÑEQUERA UNIVERSAL COMPRESSION TECH Talla 2 Color Beige
- FARMALASTIC RODILLERA CERRADA COMPRESSION TECH Talla Mediana Color Bei
- FARMALASTIC RODILLERA GONARTROSIS Talla EG Color Beige
- FARMALASTIC VENDA ELÁSTICA COHESIVA Tamaño 10 cm × 4,5 m Color Blanco
- MEDIA LARGA BLONDA (A-F) COMPRESIÓN LIGERA FARMALASTIC Color Camel Tal
Showing 12 of 330 declared devices.
Catalogue references include 0355024, 158259.1, 158427.4, 211844.7, 216163.4, 224560.0.
European nomenclature codes declared: M030405, Y060308, Y061209, Y060612, Y06120601, Y060609.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | LABORATORIOS INDAS SA (ES) · FDA 3013152936 |
| Devices in EUDAMED | 330 |
| Country of registration | Spain |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 330 |
|---|---|
| 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.