Componentes de plástico aprobados por la FDA
- Enhanced Hygiene – Reduces risk of contamination in medical settings.
- Versatility – Suitable for a wide range of applications.
- Easy to Sterilize – Can be cleaned and sanitized for reuse.
- Long-Lasting – Resistant to wear and aging.
- Consistent Quality – Ensures uniformity across production.
Detalles del producto
Componentes plásticos aprobados por la FDA se refieren a materiales plásticos que han superado las rigurosa pruebas y evaluaciones de la FDA para confirmar su seguridad y idoneidad para su uso en productos médicos, envases o dispositivos que puedan entrar en contacto con alimentos, fármacos o el cuerpo humano.
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Preguntas frecuentes
They ensure consistent quality, safety, and reliability, which are critical for the performance of medical devices and other health-related products.
Examples include plastic syringes, IV bags, medical tubing, and packaging for pharmaceutical products.
They undergo various tests, including biocompatibility, chemical stability, and performance evaluations to ensure they are safe for intended use.
FDA approved plastic parts must meet regulatory standards such as 21 CFR 177 for food packaging and 21 CFR 820 for medical devices.
FDA approved plastics have been tested and verified for specific uses, while FDA registered plastics may only be listed but not necessarily tested for those applications.



