Le couvercle médical Tyvek® est un matériau non tissé en HDPE haut de gamme destiné au scellage des dispositifs médicaux stériles. Il offre une excellente perméabilité à l’air, une barrière microbienne performante, une résistance à la déchirure et à la perforation. Il prend en charge plusieurs procédés de stérilisation et garantit un pelage propre et régulier pour préserver l’intégrité de l’emballage stérile sur le long terme.
Méthodes de stérilisation
Stérilisation à l’oxyde d’éthylène
Irradiation gamma
Stérilisation par faisceau d’électrons
Stérilisation à la vapeur contrôlée
Caractéristiques
Excellente barrière microbienne
Haute résistance à la déchirure et à la perforation
Pelage propre et stable
Faible émission de particules, sans peluche
Technologie de scellant
Revêtement thermofusible uniforme
Résistance de thermoscellage stable
Pelage sans résidu
Compatible avec le scellage complet du bord du plateau
Matériaux disponibles
Tyvek® 1073B grade médical
Tyvek® 2FS haute performance
Fibre non tissée HDPE vierge
Grade médical 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.
