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Zymo Research recibe la aprobación 510(k) para su dispositivo de recolección/transporte para la COVID-19
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El primer medio de transporte con aprobación 510(k) para pruebas de COVID-19

Zymo Research Corp. Logo

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Zymo Research Corp.

Mar 11, 2021, 16:31 ET

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IRVINE, California, 11 de marzo de 2021 /PRNewswire/ -- Zymo Research anunció hoy que la Administración de Alimentos y Medicamentos de los Estados Unidos (FDA) ha aprobado su tubo de recolección DNA/RNA Shield™ como dispositivo médico clase II. La aprobación 510(k) de la FDA autoriza el uso del producto como dispositivo de diagnóstico in vitro (IVD) para pruebas de COVID-19.

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La FDA aprueba el tubo de recolección DNA/RNA Shield™ de Zymo Research como dispositivo médico clase& II. La aprobación 510(k) de la FDA autoriza el uso del producto como dispositivo de diagnóstico in vitro (IVD) para pruebas de COVID-19. (PRNewsfoto/Zymo Research Corp.)
La FDA aprueba el tubo de recolección DNA/RNA Shield™ de Zymo Research como dispositivo médico clase& II. La aprobación 510(k) de la FDA autoriza el uso del producto como dispositivo de diagnóstico in vitro (IVD) para pruebas de COVID-19. (PRNewsfoto/Zymo Research Corp.)

Específicamente aprobada para pruebas de COVID-19, el dispositivo de recolección DNA/RNA Shield™ es la primera tecnología autorizada por la FDA que inactiva el virus y preserva el ARN del SARS-CoV-2. El virus SARS-CoV-2 se inactiva de manera efectiva, lo que permite manipular, transportar y almacenar la muestra de manera segura. Esto garantiza la seguridad de los trabajadores en la primera línea de la salud y laboratorios. El ARN viral se estabiliza a temperatura ambiente por períodos prolongados para un análisis robusto a través de ensayos de RT-PCR.

"DNA/RNA Shield ya tenía un historial comprobado en varias aplicaciones de enfermedades infecciosas antes de la pandemia actual, esto facilitó su rápida adopción e implementación en las primeras etapas del brote de COVID", afirmó el Dr. Marc Van Eden, vicepresidente de Desarrollo de Negocios de Zymo Research. "La 510(k) es el resultado de la colaboración activa de la FDA con Zymo Research para posicionar esta tecnología a la vanguardia de las pruebas actuales y los futuros esfuerzos de vigilancia".

El producto consiste en un tubo que contiene el medio de transporte patentado DNA/RNA Shield™ de Zymo Research. El medio de transporte garantiza la estabilidad del ARN SARS-CoV-2 durante el transporte y almacenamiento de muestras hasta por 28 días a temperaturas ambiente. El medio de transporte DNA/RNA Shield™ puede ser parte de un kit junto a un hisopo o un kit de recolección de flemas, o presentarse como un tubo independiente.

La tecnología es compatible con muestras humanas del sistema respiratorio superior e inferior con sospecha de contener SARS-CoV-2. Los especímenes recolectados y almacenados en un tubo de recolección DNA/RNA Shield™ son aptos para su uso en pruebas de diagnóstico molecular adecuadas.

Para obtener más información, visite el sitio web de Zymo Research o comuníquese con ellos por correo electrónico al [email protected].

Acerca de Zymo Research Corp.

Zymo Research es una compañía privada que presta servicios a la comunidad científica y de diagnóstico con herramientas de biología molecular de última generación desde 1994. "La belleza de la ciencia es simplificar las cosas" es su lema, que se refleja en todos sus productos, desde la epigenética hasta las tecnologías de purificación de ADN/ARN. Históricamente reconocida como líder en epigenética, Zymo Research está rompiendo barreras con innovadoras soluciones para la recolección de muestras, mediciones microbiómicas, dispositivos de diagnóstico y tecnologías de secuenciación de nueva generación (NGS) de alta calidad y fáciles de usar. Siga a Zymo Research en Facebook, LinkedIn, Twitter e Instagram.

Para obtener más información sobre los productos de Zymo Research para la COVID-19, consulte los siguientes enlaces:

  • Zymo Research lanza software gratuito para agilizar las pruebas de COVID-19
  • Zymo Research obtiene el marcado CE IVD para su Quick SARS-CoV-2 Multiplex Kit
  • Zymo Research obtiene la autorización de uso de emergencia de la FDA para su Quick SARS-CoV-2 rRT-PCR Kit
  • Zymo Research recibe el marcado CE IVD para su Quick-DNA/RNA™ Viral MagBead Kit
  • Zymo Research lanza un servicio de secuenciación de COVID-19 para la detección y vigilancia de variantes emergentes del SARS-CoV-2
  • Zymo Research ofrece detección de SARS-CoV-2 y rastreo de variantes a nivel comunitario con el servicio de pruebas en aguas residuales Environ™ COVID-19

Fotografía: https://mma.prnewswire.com/media/1454412/510K_Shield_FDA_Certified_PR_2000x1111px_v2.jpg

Logotipo: https://mma.prnewswire.com/media/364743/Zymo_Research_Corp_Logo.jpg

FUENTE Zymo Research Corp.

Related Links

http://www.zymoresearch.com

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