Les couvercles barrières en aluminium sont des opercules d’emballage médical à haute barrière. Ils bloquent efficacement l’humidité, l’oxygène et la lumière pour assurer une protection durable des médicaments et des dispositifs médicaux sensibles. Leur excellente barrière et leur scellage stable permettent de prolonger la durée de conservation des produits.
Méthodes de stérilisation
Stérilisation à l’oxyde d’éthylène
Stérilisation par rayonnement gamma
Stérilisation par faisceau d’électrons
Stérilisation à chaleur sèche
Caractéristiques produit
Haute performance barrière
Résistance à l’humidité et à l’oxygène
Protection anti-lumière
Prolonge la durée de conservation
Technologie de scellage
Couche thermoscellable de grade médical
Résistance de scellage stable
Pelage propre sans résidu
Résistance aux hautes températures
Compatibilité des supports
Matériau composite aluminium
Plateaux PVC / PP / PET / PS
Blister pharmaceutique
Dimensions et structure personnalisées
ABOUT FACTORY
WELCOME TO BEST INDUSTRIAL BUSINESS
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.
