5. STROKE ARRAY MARCA: RANDOX
- Risk class / Clase de Riesgo
- I
- Product type (Spanish)
- REACTIVOS IN VITRO
- Product type (English)
- REACTIVOS IN VITRO
- Analysis ID
- 81288170151afeaf11bc055b97ae2dd5
- Expire date
- February 22, 2034
- Name (Spanish)
- BIOLORE LTDA
- Name (English)
- BIOLORE LTDA
EL EVIDENCE MULTISTAT STROKE ARRAY SE DEBE UTILIZAR PARA SÓLO PARA USO EN INVESTIGACIÓN Y NO PARA USO EN DIAGNÓSTICO._x000D_ PROCEDIMIENTOS PARA LA DETECCIÓN CUANTITATIVA SIMULTÁNEA DE STNFR1, FABP3, DÍMERO D, PARK7, NDKA, GFAP, GSTPI Y IL-6 DE UNA ÚNICA MUESTRA DE_x000D_ PLASMA.
THE EVIDENCE MULTISTAT STROKE ARRAY SHOULD BE USED FOR RESEARCH USE ONLY AND NOT FOR DIAGNÓSTICO._x000D_ PROCEDURES FOR THE SIMULTANEOUS QUANTITATIVE DETECTION OF STNFR1, FABP3, D-DIMER, PARK7, NDKA, GFAP, GSTPI, AND IL-6 FROM A SINGLE SAMPLE DE_x000D_ PLASMA.
Access comprehensive regulatory information for 5. STROKE ARRAY MARCA: RANDOX (5. STROKE ARRAY MARCA: RANDOX) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 81288170151afeaf11bc055b97ae2dd5 and manufactured by BIOLORE LTDA. The device was registered on February 22, 2034.
This page provides complete registration details including product type (REACTIVOS IN VITRO), authorised information, and regulatory compliance data from the official Colombia INVIMA medical device database. Pure Global AI offers free access to Colombia's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate INVIMA regulations efficiently.