Notre lidstock papier médical est un matériau de barrière stérile destiné aux plateaux médicaux thermoformés, blisters et récipients rigides médicaux. Il offre une barrière microbienne stable, une résistance à l’humidité maîtrisée et une thermoscellure pelable fiable. Validé pour les cycles de stérilisation, il préserve l’intégrité de l’emballage et maintient la stérilité des dispositifs médicaux durant le stockage et la distribution.
Applications
Plateaux médicaux thermoformés
Blisters médicaux
Récipients rigides jetables
Emballage de consommables stériles
Performances clés
Papier respirant qualité médicale
Barrière microbienne fiable
Résistance à l’humidité maîtrisée
Peu de peluches, pelage propre
Technologie de scellage
Revêtement de thermoscellage médical
Résistance de scellage constante
Pelable, sans résidu de colle
Compatible avec plusieurs supports
Matériau & personnalisation
Papier base cellulose médical
Papier enduit PE / EAA
Compatible plateaux PVC / PP / PET / PS
Taille, impression et découpe sur mesure
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.
