Der Tyvek® medizinische Deckelfilm ist ein hochwertiges HDPE-Vliesmaterial zum Versiegeln steriler Medizinprodukte. Er überzeugt durch ausgezeichnete Luftdurchlässigkeit, eine starke Mikrobenbarriere sowie hohe Reiß- und Durchstichfestigkeit. Er ist für verschiedene Sterilisationsverfahren geeignet und bietet eine gleichmäßige saubere Ablösung, um die Integrität der sterilen Verpackung langfristig zu sichern.
Sterilisationsverfahren
EtO-Sterilisation
Gamma-Bestrahlung
Elektronenstrahlsterilisation
Gesteuerte Dampfsterilisation
Eigenschaften
Hervorragende Mikrobenbarriere
Hohe Reiß- und Durchstichfestigkeit
Stabile saubere Ablösung
Partikelarm, fusselfrei
Siegellack-Technologie
Gleichmäßige Heißschmelzbeschichtung
Stabile Heißsiegelkraft
Rückstandsfreie Ablösung
Kompatibel mit vollständiger Randversiegelung
Verfügbare Materialien
Tyvek® 1073B medizinische Qualität
Tyvek® 2FS Hochleistungsqualität
Neues HDPE-Vliesfasermaterial
Biokompatible medizinische Qualität
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.
