IMTEC-ANA SCREEN
- Risk class / Clase de Riesgo
- II
- Product type (Spanish)
- REACTIVO DIAGNOSTICO
- Product type (English)
- DIAGNOSTIC REAGENT
- Analysis ID
- 7f6abd71b9c4aaf691de6977e7e64514
- Expire date
- January 27, 2032
- Name (Spanish)
- HUMAN GESELLSCHAFT FÜR BIOCHEMICA UND DIAGNOSTICA MBH
- Name (English)
- HUMAN GESELLSCHAFT FÜR BIOCHEMICA UND DIAGNOSTICA MBH
DETERMINACIÓN DE LOS DIFERENTES ANALITOS RELACIONADOS CON MUESTRAS PROCEDENTES DEL ORGANISMO HUMANO.
DETERMINATION OF THE DIFFERENT ANALYTES RELATED TO SAMPLES FROM THE HUMAN ORGANISM.
Access comprehensive regulatory information for IMTEC-ANA SCREEN (IMTEC-ANA SCREEN) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 7f6abd71b9c4aaf691de6977e7e64514 and manufactured by HUMAN GESELLSCHAFT FÜR BIOCHEMICA UND DIAGNOSTICA MBH. The device was registered on January 27, 2032.
This page provides complete registration details including product type (DIAGNOSTIC REAGENT), 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.