BLOOD TRANSFUSION SET - Argentina Medical Device Registration
Access comprehensive regulatory information for BLOOD TRANSFUSION SET in the Argentina medical device market through Pure Global AI's free database. This Class I-II Registration medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on February 14, 2024.
This page provides complete registration details including product code (1440-63), brand name (MCM, SQL, EUROMIX, EUROCARE, BIOSWISS), authorized representative information, registration type, and regulatory compliance data from the official Argentina ANMAT medical device database. Pure Global AI offers free access to Argentina's medical device registry, helping global MedTech companies navigate Argentina regulations efficiently.
BLOOD TRANSFUSION SET (SINGLE/DOUBLE CHAMBER, WITH/WITHOUT VENTILATION); BLOOD TRANSFUSION SET WITH Y/NO NEEDLE-INJECTING PORT VENTILATION: BLOOD TRANSFUSION SET WITH/WITHOUT VENTILATION, WITH LATÉX LUER SLIP BULB WITH/WITHOUT NEEDLE; BLOOD TRANSFUSION SET WITH/WITHOUT LUER LOCK IN PLACE AND WITH/WITHOUT NEEDLE.
SET PARA TRANSFUSION DE SANGRE (CAMARA SIMPLE/DOBLE , CON/SIN VENTILACIÓN); SET PARA TRANSFUSION DE SANGRE CON VENTILACION EN PUERTO DE INYECCIÓN EN Y CON/SIN AGUJA: SET PARA TRANSFUSION DE SANGRE CON/SIN VENTILACIÓN, CON BULBO LATÉX LUER SLIP CON/SIN AGUJA; SET PARA TRANSFUSION DE SANGRE CON/SIN CON BLOQUEO LUER LOCK EN SITIO Y CON/SIN AGUJA.