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Esto es a ra\u00edz que existe en el mercado equipos de altas gamas que realizan m\u00e1s pruebas en simult\u00e1neo, como por ejemplo hasta 12 pruebas, lo que ser\u00eda beneficioso para el hospital utilizar el equipo en varios pacientes al mismo tiempo. ", "author": {"name": "EUROQUIMICA S.A.", "id": "PY-RUC-80061211-6"}, "answer": "Se solicita a los oferentes remitirse a lo requerido en el pliego de bases y condiciones por la convocante, la misma se realiza en base a las necesidades de los servicios, que han solicitado realizar 4 pruebas por pacientes, la naturaleza de la tecnolog\u00eda solicitada es espec\u00edfica para monitoreo de pacientes sangrando y/o monitoreo de pacientes espec\u00edficos que tengan riesgos de sangrar por su patolog\u00eda o intervenci\u00f3n, hace que no sea una prueba de monitoreo masivo que requiera tecnolog\u00eda en raz\u00f3n a n\u00famero de pacientes en bloque.", "dateAnswered": "2022-10-10T14:59:01-04:00"}, {"id": "4", "date": "2022-10-06T10:12:32-04:00", "title": "ALMACENAMIENTO DE LOS REACTIVOS", "description": "En el Pliego de Bases y Condiciones, en las Especificaciones t\u00e9cnicas solicitan que los Reactivos sean almacenados a Temperatura ambiente, por tal motivo solicitamos a la convocante que permita como opci\u00f3n que los reactivos sean refrigerados de 2 a 8 grados, ya que los mismos no afectara la estabilidad ni sensibilidad de los reactivos indistintamente al tipo de almacenamiento.  ", "author": {"name": "EUROQUIMICA S.A.", "id": "PY-RUC-80061211-6"}, "answer": "Favor remitirse a lo establecido en las especificaciones t\u00e9cnicas del pliego de bases y condiciones, teniendo en cuenta que el almacenamiento de los insumos de manera simple y b\u00e1sica sin condiciones t\u00e9rmicas especificas garantizan la adecuada preservaci\u00f3n de estos y su f\u00e1cil manejo.  Los riesgos de tener insumos refrigerados son altos en raz\u00f3n a la log\u00edstica de la cadena de frio, las fluctuaciones de voltaje, la ausencia de sistemas adecuados de refrigeraci\u00f3n etc., que conllevan a la perdida de los mismos.", "dateAnswered": "2022-10-10T14:57:59-04:00"}, {"id": "3", "date": "2022-10-06T10:11:16-04:00", "title": "PRESENTACI\u00d3N \u0096 ESPECIFICACIONES TECNICAS", "description": "Podr\u00eda la convocante ampliar la presentaci\u00f3n requerida de Cartuchos de un solo uso a Reactivos para analizadores de sangre, teniendo en cuenta que denominarlo como Cartucho imposibilitar\u00eda el poder cotizar otros tipos de presentaciones existentes en el mercado nacional como ampollas y/o viales de distintas clases, as\u00ed como tambi\u00e9n el oferente que cuente con Cartuchos de igual manera podr\u00eda cotizar denomin\u00e1ndolo de esta forma. Esta ampliaci\u00f3n no afectar\u00eda con todo lo solicitado en el Pliego de Bases y Condiciones de cumplir con la detecci\u00f3n de hiperfibrin\u00f3lisis, coagulopat\u00edas por diluci\u00f3n, sustituci\u00f3n de fibrin\u00f3geno, factores o sustituci\u00f3n de plaquetas, as\u00ed como el control de la dosis de heparina o protamina", "author": {"name": "EUROQUIMICA S.A.", "id": "PY-RUC-80061211-6"}, "answer": "Se solicita a los oferentes  ajustarse a lo establecido en las especificaciones t\u00e9cnicas del Pliego de Bases y Condiciones, teniendo en cuenta dicha modalidad de diagn\u00f3stico se realiza con una unidad port\u00e1til en las unidades quir\u00fargicas ( Quir\u00f3fanos), ya con este desarrollo tecnol\u00f3gico se evita los m\u00faltiples pasos,  con m\u00ednima intervenci\u00f3n por parte del usuario final, desde la toma de muestra al resultado, por lo que se necesita de la tecnolog\u00eda Cartucho \u00fanico (unicomponente) que contenga todos y cada uno de los reactivos que requiere el proceso total de la muestra.", "dateAnswered": "2022-10-10T14:54:38-04:00"}, {"id": "2", "date": "2022-10-05T18:19:14-04:00", "title": "Sistema de Adjudicaci\u00f3n", "description": "En vista que la convocante ha decidido realizar el sistema de adjudicaci\u00f3n por \u00edtems y dentro de ambos \u00edtems (N\u00b0 1 y N\u00b0 2) est\u00e1n destinados para los mismos hospitales (HOSPITAL MATERNO INFANTIL SAN PABLO, HOSPITAL DE TRAUMA, HOSPITAL GENERAL PEDIATRICO, INSTITUTO NACIONAL DE CARDIOLOGIA). Consideramos m\u00e1s conveniente que la convocante opte por el sistema de Adjudicaci\u00f3n por Lote para Cada Hospital. De esta forma se ampliara a mayor participaci\u00f3n obteniendo ventajas competitivas en cuanto al precio de lo solicitado.   ", "author": {"name": "PROSALUD FARMA S.A.", "id": "PY-RUC-80033584-8"}, "answer": "Los oferentes deber\u00e1n ajustarse al PBC, teniendo en cuenta las necesidades de los servicios, as\u00ed como la especificidad y complejidad de los mismos, por tanto, se mantiene el requerimiento del sistema de adjudicaci\u00f3n\n\n ", "dateAnswered": "2022-10-10T14:56:22-04:00"}, {"id": "6", "date": "2022-10-06T10:28:11-04:00", "title": "DE ITEMS A LOTES", "description": "En el Pliego de Bases y Condiciones, la convocante ha optado por el sistema de Adjudicaci\u00f3n de \u00edtems, siendo los dos \u00edtems para los mismos hospitales Hospital Materno Infantil San Pablo, Hospital De Trauma, Hospital General Pedi\u00e1trico, Instituto Nacional De Cardiolog\u00eda y as\u00ed tambi\u00e9n los mismos requerimientos salvo que en uno solicitan el control de dosis de heparina. Por lo que teniendo en cuenta los equipos disponibles en el mercado y las funcionalidades de los mismos, no habr\u00eda inconveniente en unificar los requerimientos y realizarlos por lotes por Hospitales, generando practicidad para la convocante como mayor oportunidad a oferentes interesados.  ", "author": {"name": "EUROQUIMICA S.A.", "id": "PY-RUC-80061211-6"}, "answer": "Los oferentes deber\u00e1n ajustarse al PBC, teniendo en cuenta las necesidades de los servicios, as\u00ed como la especificidad y complejidad de los mismos, por tanto, se mantiene el requerimiento del sistema de adjudicaci\u00f3n\n\n ", "dateAnswered": "2022-10-10T14:56:38-04:00"}, {"id": "9", "date": "2022-10-07T00:26:05-04:00", "title": "Especificaciones Tecnicas", "description": "2 Especificaciones Tecnicas:\nCartuchos de un solo uso con 1 (un) equipo en comodato, para la determinaci\u00f3n por medio del \nTest Viscoelastico con capacidad de realizar el an\u00e1lisis global de la coagulaci\u00f3n sangu\u00ednea, que\npermita evaluar en forma r\u00e1pida la hemostasia general del paciente, con capacidad de detectar\nhiperfibrin\u00f3lisis, coagulopat\u00edas por diluci\u00f3n, sustituci\u00f3n de fibrin\u00f3geno, factores o sustituci\u00f3n\nde plaquetas.\nConsulta: \nLos cartuchos solicitados de un solo uso para realiziaar la determinaciones de an\u00e1lisis global de la coagulaci\u00f3n sangu\u00ednea, que\npermita evaluar en forma r\u00e1pida la hemostasia general del paciente, con capacidad de detectar\nhiperfibrin\u00f3lisis, coagulopat\u00edas por diluci\u00f3n, sustituci\u00f3n de fibrin\u00f3geno, factores o sustituci\u00f3n\nde plaquetas deben incluir en un solo cartucho?\nFavor aclara si es necesario 1 Cartucho para: an\u00e1lisis global de la coagulaci\u00f3n sangu\u00ednea\n1 Cartucho para detectar\nhiperfibrin\u00f3lisis\n1 cartucho para detectar coagulopat\u00edas por diluci\u00f3n\n1 cartucho para sustitucion de Fibrinogeno\n1 Cartucho para Factores o sustitucion de plaquetas\n", "author": {"name": "G T SCIENTIFIC S.A.", "id": "PY-RUC-80000084-6"}, "answer": "Se solicita a los oferentes  ajustarse a lo establecido en las especificaciones t\u00e9cnicas del Pliego de Bases y Condiciones, teniendo en cuenta dicha modalidad de diagn\u00f3stico se realiza con una unidad port\u00e1til en las unidades quir\u00fargicas ( Quir\u00f3fanos), ya con este desarrollo tecnol\u00f3gico se evita los m\u00faltiples pasos,  con m\u00ednima intervenci\u00f3n por parte del usuario final, desde la toma de muestra al resultado, por lo que se necesita de la tecnolog\u00eda Cartucho \u00fanico (unicomponente) que contenga todos y cada uno de los reactivos que requiere el proceso total de la muestra.", "dateAnswered": "2022-10-10T14:55:02-04:00"}, {"id": "1", "date": "2022-10-05T18:18:38-04:00", "title": "Especificaciones T\u00e9cnicas", "description": "Solicitamos a la convocante modificar la presentaci\u00f3n de Cartuchos a Reactivos para analizadores de sangre, teniendo en cuenta que en el mercado existen reactivos de distintas presentaciones tales como: cartuchos, viales liquidas y viales liofilizadas y que de igual modo cuentan con la capacidad de detectar hiperfibrin\u00f3lisis, coagulopat\u00edas por diluci\u00f3n, sustituci\u00f3n de fibrin\u00f3geno, factores o sustituci\u00f3n de plaquetas, as\u00ed como el control de la dosis de heparina o protamina.  Esto permitir\u00e1 a la convocante contar con precios competitivos y una diversidad de opciones en cuanto a la calidad de los equipos. ", "author": {"name": "PROSALUD FARMA S.A.", "id": "PY-RUC-80033584-8"}, "answer": "Se solicita a los oferentes  ajustarse a lo establecido en las especificaciones t\u00e9cnicas del Pliego de Bases y Condiciones, teniendo en cuenta dicha modalidad de diagn\u00f3stico se realiza con una unidad port\u00e1til en las unidades quir\u00fargicas ( Quir\u00f3fanos), ya con este desarrollo tecnol\u00f3gico se evita los m\u00faltiples pasos,  con m\u00ednima intervenci\u00f3n por parte del usuario final, desde la toma de muestra al resultado, por lo que se necesita de la tecnolog\u00eda Cartucho \u00fanico (unicomponente) que contenga todos y cada uno de los reactivos que requiere el proceso total de la muestra.", "dateAnswered": "2022-10-10T14:54:21-04:00"}, {"id": "8", "date": "2022-10-07T00:23:52-04:00", "title": "muestras", "description": "Consulta:  En las especificaciones tecnicas estan pidiendo:\nCartuchos de un solo uso con 1 (un) equipo en comodato, para la determinaci\u00f3n por medio del \nTest Viscoelastico con capacidad de realizar el an\u00e1lisis global de la coagulaci\u00f3n sangu\u00ednea, que\npermita evaluar en forma r\u00e1pida la hemostasia general del paciente, con capacidad de detectar\nhiperfibrin\u00f3lisis, coagulopat\u00edas por diluci\u00f3n, sustituci\u00f3n de fibrin\u00f3geno, factores o sustituci\u00f3n\nde plaquetas. Con certificado de calidad FDA o ISO o CE. Con provisi\u00f3n de Equipo totalmente\nautomatizado, sin pipeteo ni preparacion de pruebas en COMODATO.\nEsto se refiere a presentar los cartuchos y el equipo que debe de ponerse en comodato?\nEstos cartuchos y equipos en comodato tienen un costo muy elevado, tanto el cartucho como el equipo, solicitamos que solo se presente los folletos tanto de los cartuchos como de los equipos en comodato.\n", "author": {"name": "G T SCIENTIFIC S.A.", "id": "PY-RUC-80000084-6"}, "answer": "Los documentos mencionados forman parte de los requisitos de capacidad t\u00e9cnica, teniendo en cuenta la funci\u00f3n de la convocante salvaguardar los intereses de la instituci\u00f3n, establece que conforme atribuciones del Comit\u00e9 de Evaluaci\u00f3n, si lo considera necesario solicitar\u00e1 las muestras a los oferentes en concurso. Solicitamos a los oferentes remitirse a lo establecido en el Pliego de Bases y Condiciones", "dateAnswered": "2022-10-10T14:59:41-04:00"}, {"id": "7", "date": "2022-10-07T00:20:07-04:00", "title": "muestras", "description": "Muestras\nEn atenci\u00f3n a que en el llamado de referencia la convocante requiere para los \u00edtems  Reactivos  para uso en  Laboratorio de An\u00e1lisis   solicitamos a la convocante que para el \u00edtem mencionado la convocante permita presentar   la insertos y/o cat\u00e1logos /especificaciones t\u00e9cnicas del fabricante correspondiente al reactivo ofertado en reemplazo de las muestras considerando estos  documentos son v\u00e1lidos con el cual el comit\u00e9 evaluador podr\u00eda claramente avalar el cumplimiento de las especificaciones t\u00e9cnicas solicitadas en el PBC y  usualmente son solicitados en los llamados para reactivos. Teniendo en cuenta la naturaleza de este tipo de producto y son los documentos que permiten evaluar las caracter\u00edsticas t\u00e9cnicas en los llamados de  reactivos\n", "author": {"name": "G T SCIENTIFIC S.A.", "id": "PY-RUC-80000084-6"}, "answer": "Los documentos mencionados forman parte de los requisitos de capacidad t\u00e9cnica, teniendo en cuenta la funci\u00f3n de la convocante salvaguardar los intereses de la instituci\u00f3n, establece que conforme atribuciones del Comit\u00e9 de Evaluaci\u00f3n, si lo considera necesario solicitar\u00e1 las muestras a los oferentes en concurso. Solicitamos a los oferentes remitirse a lo establecido en el Pliego de Bases y Condiciones.", "dateAnswered": "2022-10-10T14:59:35-04:00"}, {"id": "10", "date": "2022-10-07T00:27:52-04:00", "title": "Especificaciones Tecnicas", "description": "Especificaciones Tecnicas\nEquipo totalmente\nautomatizado, sin pipeteo ni preparacion de pruebas\nConsulta: A que se refiere con equipo totalmente automatizado sin pipeteo ni preparacion de muestras?\nEn el mercado solo exiten 2 analizadores para est Viscoelastico \nUno de ellos se encastra directamente el tubo de muestra en el cartucho y este analizador es el ROTEM Sigma.\nEl otro equipo es el Analizador Igual o mejor que el Rotem Sigma pero este se debe dispensar de los tubos de muestra a los cartuchos.\nSolicitamos a la convocante incluir las dos modalidades para dar participacion a otro oferente o de lo contrario estas especificaciones solo son para el Rotem Sigma\n", "author": {"name": "G T SCIENTIFIC S.A.", "id": "PY-RUC-80000084-6"}, "answer": "Se solicita a los oferentes  ajustarse a lo establecido en las especificaciones t\u00e9cnicas del Pliego de Bases y Condiciones, teniendo en cuenta dicha modalidad de diagn\u00f3stico se realiza con una unidad port\u00e1til en las unidades quir\u00fargicas ( Quir\u00f3fanos), ya con este desarrollo tecnol\u00f3gico se evita los m\u00faltiples pasos,  con m\u00ednima intervenci\u00f3n por parte del usuario final, desde la toma de muestra al resultado, por lo que se necesita de la tecnolog\u00eda Cartucho \u00fanico (unicomponente) que contenga todos y cada uno de los reactivos que requiere el proceso total de la muestra.", "dateAnswered": "2022-10-10T14:55:13-04:00"}, {"id": "11", "date": "2022-10-07T00:30:42-04:00", "title": "Especificaciones tecnicas", "description": "4 Especificaciones tecnicas\nEl tubo de la muestra debe caber directamente en el\ncartucho\nConsulta: Esta especificacion es exclusivo del analizador Rotem Sigma.\nSolicitamos a la convocante incluir tambien la opcion de Pipetear la muestra en el cartucho, ya que este paso no afecta la calidad de los resultados ni tampoco se puede obtener errores de lectura, asi para dar mayor participacion a otros oferentes\n", "author": {"name": "G T SCIENTIFIC S.A.", "id": "PY-RUC-80000084-6"}, "answer": "Se solicita a los oferentes  ajustarse a lo establecido en las especificaciones t\u00e9cnicas del Pliego de Bases y Condiciones, teniendo en cuenta dicha modalidad de diagn\u00f3stico se realiza con una unidad port\u00e1til en las unidades quir\u00fargicas ( Quir\u00f3fanos), ya con este desarrollo tecnol\u00f3gico se evita los m\u00faltiples pasos,  con m\u00ednima intervenci\u00f3n por parte del usuario final, desde la toma de muestra al resultado, por lo que se necesita de la tecnolog\u00eda Cartucho \u00fanico (unicomponente) que contenga todos y cada uno de los reactivos que requiere el proceso total de la muestra.", "dateAnswered": "2022-10-10T14:55:26-04:00"}], "lots": [{"id": "n2IFswHbMPE=", "title": "1 - 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