El lidstock médico Tyvek® es un material no tejido de HDPE de alta gama, diseñado para el sellado de dispositivos médicos estériles. Cuenta con excelente transpirabilidad, barrera microbiana superior, resistencia al desgarro y a la perforación, admite múltiples procesos de esterilización y ofrece un despegue limpio constante para conservar la integridad del empaque estéril a largo plazo.
Métodos de esterilización
Esterilización por óxido de etileno
Radiación gamma
Esterilización por haz de electrones
Esterilización por vapor controlado
Características
Barrera microbiana superior
Alta resistencia al desgarro y perforación
Despegue limpio estable
Baja generación de partículas, sin pelusa
Tecnología de sellante
Recubrimiento uniforme de termofusible
Resistencia de termosellado estable
Despegue sin residuos
Compatible con sellado total del borde de la bandeja
Materiales disponibles
Tyvek® 1073B grado médico
Tyvek® 2FS alto rendimiento
Fibra no tejida HDPE virgen
Grado médico biocompatible
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Martin provides 100% medical-grade virgin PETG blister trays produced in dust-free workshop. All materials have complete certification documents, stable batch consistency, and support customized deep-drawing, multi-cavity, anti-shake and anti-static structures.
ISO 11607, EN 868, GB/T 19633
Additional applicable standards:
[1] GB/T 19633‑2005 Packaging for terminally sterilized medical devices
[2] GB/T 5402‑2003 Paper and board — Determination of air permeance (medium range) — Gurley method
[3] ISO/DIS 22611 Clothing for protection against infectious agents — Test method for resistance to penetration by microbial‑containing aerosols
[4] ASTM F 1980 Standard Guide for Accelerated Aging of Sterile Medical Device Packages
ISO 11607, EN 868, GB/T 19633
Additional applicable standards:
[1] GB/T 19633‑2005 Packaging for terminally sterilized medical devices
[2] GB/T 5402‑2003 Paper and board — Determination of air permeance (medium range) — Gurley method
[3] ISO/DIS 22611 Clothing for protection against infectious agents — Test method for resistance to penetration by microbial‑containing aerosols
[4] ASTM F 1980 Standard Guide for Accelerated Aging of Sterile Medical Device Packages
ISO 11607, EN 868, GB/T 19633
Additional applicable standards:
[1] GB/T 19633‑2005 Packaging for terminally sterilized medical devices
[2] GB/T 5402‑2003 Paper and board — Determination of air permeance (medium range) — Gurley method
[3] ISO/DIS 22611 Clothing for protection against infectious agents — Test method for resistance to penetration by microbial‑containing aerosols
[4] ASTM F 1980 Standard Guide for Accelerated Aging of Sterile Medical Device Packages
ISO 11607, EN 868, GB/T 19633
Additional applicable standards:
[1] GB/T 19633‑2005 Packaging for terminally sterilized medical devices
[2] GB/T 5402‑2003 Paper and board — Determination of air permeance (medium range) — Gurley method
[3] ISO/DIS 22611 Clothing for protection against infectious agents — Test method for resistance to penetration by microbial‑containing aerosols
[4] ASTM F 1980 Standard Guide for Accelerated Aging of Sterile Medical Device Packages
ISO 11607, EN 868, GB/T 19633
Additional applicable standards:
[1] GB/T 19633‑2005 Packaging for terminally sterilized medical devices
[2] GB/T 5402‑2003 Paper and board — Determination of air permeance (medium range) — Gurley method
[3] ISO/DIS 22611 Clothing for protection against infectious agents — Test method for resistance to penetration by microbial‑containing aerosols
[4] ASTM F 1980 Standard Guide for Accelerated Aging of Sterile Medical Device Packages
ISO 11607, EN 868, GB/T 19633
Additional applicable standards:
[1] GB/T 19633‑2005 Packaging for terminally sterilized medical devices
[2] GB/T 5402‑2003 Paper and board — Determination of air permeance (medium range) — Gurley method
[3] ISO/DIS 22611 Clothing for protection against infectious agents — Test method for resistance to penetration by microbial‑containing aerosols
[4] ASTM F 1980 Standard Guide for Accelerated Aging of Sterile Medical Device Packages
ISO 11607, EN 868, GB/T 19633
Additional applicable standards:
[1] GB/T 19633‑2005 Packaging for terminally sterilized medical devices
[2] GB/T 5402‑2003 Paper and board — Determination of air permeance (medium range) — Gurley method
[3] ISO/DIS 22611 Clothing for protection against infectious agents — Test method for resistance to penetration by microbial‑containing aerosols
[4] ASTM F 1980 Standard Guide for Accelerated Aging of Sterile Medical Device Packages
ISO 11607, EN 868, GB/T 19633
Additional applicable standards:
[1] GB/T 19633‑2005 Packaging for terminally sterilized medical devices
[2] GB/T 5402‑2003 Paper and board — Determination of air permeance (medium range) — Gurley method
[3] ISO/DIS 22611 Clothing for protection against infectious agents — Test method for resistance to penetration by microbial‑containing aerosols
[4] ASTM F 1980 Standard Guide for Accelerated Aging of Sterile Medical Device Packages
ISO 11607, EN 868, GB/T 19633
Additional applicable standards:
[1] GB/T 19633‑2005 Packaging for terminally sterilized medical devices
[2] GB/T 5402‑2003 Paper and board — Determination of air permeance (medium range) — Gurley method
[3] ISO/DIS 22611 Clothing for protection against infectious agents — Test method for resistance to penetration by microbial‑containing aerosols
[4] ASTM F 1980 Standard Guide for Accelerated Aging of Sterile Medical Device Packages
ISO 11607, EN 868, GB/T 19633
Additional applicable standards:
[1] GB/T 19633‑2005 Packaging for terminally sterilized medical devices
[2] GB/T 5402‑2003 Paper and board — Determination of air permeance (medium range) — Gurley method
[3] ISO/DIS 22611 Clothing for protection against infectious agents — Test method for resistance to penetration by microbial‑containing aerosols
[4] ASTM F 1980 Standard Guide for Accelerated Aging of Sterile Medical Device Packages
We have established a worldwide collaboration network, cooperating with raw material suppliers, technical institutes and distributors in over 20 countries and regions. Our cooperation centers on three core directions: co-developing medical-grade packaging materials, sharing advanced thermoforming manufacturing technology, and building a stable global supply chain to deliver custom medical packaging on schedule. We pursue win-win collaboration to achieve shared growth and sustainable value with all global partners.
