Laboratorios Conda S.A.
ES-MF-000025575 · Spain · TORREJON DE ARDOZ
Laboratorios Conda S.A. is registered in the European database on medical devices as a manufacturer, with 616 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
Among these devices, 2 are declared sterile.
Devices declared under this manufacturer
- BRAIN HEART INFUSION BROTH (BHI BROTH)
- CETRIMIDE AGAR BASE EP/USP/ISO
- CLED Agar with Andrade´s Indicator
- COLUMBIA CNA AGAR BASE
- DESOXYCHOLATE AGAR
- DNASE TEST AGAR (DEOXYRIBONUCLEASE ACTIVITY)
- E. COLI 0157:H7 CHROMOGENIC AGAR BASE
- LISTERIA FRASER BROTH BASE ISO
- LOWENSTEIN JENSEN MEDIUM (LONG TUBE)
- MACCONKEY AGAR EP/USP/ISO
- MULLER KAUFFMANN BROTH BASE
- REAGENT 1. N-ACETYL-L-CYSTEINE
Showing 12 of 616 declared devices.
Catalogue references include 1028, 1052, 1080, 1130, 1182, 1303.
European nomenclature codes declared: W0104010101, W0104010104, W0104010206, W0104010306, W0104010499, W0104010501.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | LABORATORIOS INDAS SA (ES) · FDA 3013152936 |
| Devices in EUDAMED | 616 |
| 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 | 616 |
|---|---|
| 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.