{"id":8915,"date":"2025-12-05T14:57:48","date_gmt":"2025-12-05T06:57:48","guid":{"rendered":"https:\/\/zjbocon.com\/?p=8915"},"modified":"2025-12-24T09:59:03","modified_gmt":"2025-12-24T01:59:03","slug":"sterilization-compatibility-table-for-medical-packaging-materials","status":"publish","type":"post","link":"https:\/\/zjbocon.com\/?p=8915","title":{"rendered":"Sterilization Compatibility Table for Medical Packaging Materials"},"content":{"rendered":"\n
\"\"<\/figure><\/div>\n\n\n\n
Matériel<\/strong><\/td>VAPEUR (au moins une partie de l’emballage doit être perméable à la vapeur)<\/strong><\/td>EO\/FORM (at least a part of the packaging needs to be permeable to gas)<\/strong><\/td>Peroxyde d'hydrogène (Plasma) (les matériaux à base de fibres naturelles sont incompatibles)<\/strong><\/td>Gamma\/E-Beam or Beta radiation (impermeable material may be used)<\/strong><\/td>Chaleur sèche (température maximale) (un matériau imperméable peut être utilisé)<\/strong><\/td><\/tr><\/thead>
Matériaux perméables aux gaz et à la vapeur<\/strong><\/td><\/td><\/td><\/td><\/td><\/td><\/tr>
Papier de qualité médicale<\/td>V<\/td>V<\/td>Non<\/td>V<\/td>V ($160^{\\circ}C$)<\/td><\/tr>
Matériaux non tissés filés-liés en polyéthylène<\/td>V (max. T $127^{\\circ}C$) not suitable for hospitals<\/td>V<\/td>V<\/td>V<\/td>Non<\/td><\/tr>
Non-tissés mouillés (pâte et fibres plastiques)<\/td>V<\/td>V<\/td>Non<\/td>V<\/td>Non<\/td><\/tr>
Matériaux non tissés SMS (Spunbond Meltblown Spunbond) en polypropylène<\/td>V<\/td>V<\/td>V<\/td>Non<\/td>Non<\/td><\/tr>
Films et films composites<\/strong><\/td><\/td><\/td><\/td><\/td><\/td><\/tr>
PET\/PP films (Laminated)<\/td>V<\/td>V<\/td>V<\/td>Non<\/td>Non<\/td><\/tr>
PET\/PE films (Laminated)<\/td>Non<\/td>V<\/td>V<\/td>V<\/td>Non<\/td><\/tr>
Stratifiés et composites d'aluminium, c'est-à-dire des matériaux à haute barrière<\/td>V<\/td>V<\/td>voir spécifications des fournisseurs<\/td>V<\/td>V<\/td><\/tr>
Film APET (Polyéthylène Téréphtalate Amorphe)<\/td>Non<\/td>V<\/td>voir spécifications des fournisseurs<\/td>V<\/td>Non<\/td><\/tr>
E\/P (Ethylene-Propylene Copolymer)<\/td>voir spécifications des fournisseurs<\/td>V<\/td>voir spécifications des fournisseurs<\/td>voir spécifications des fournisseurs<\/td>voir spécifications des fournisseurs<\/td><\/tr>
Film HDPE (Polyéthylène Haute Densité)<\/td>V ($121^{\\circ}C$)<\/td>V<\/td>voir spécifications des fournisseurs<\/td>V<\/td>Non<\/td><\/tr>
Film LDPE (Polyéthylène Basse Densité)<\/td>Non<\/td>V<\/td>V<\/td>V<\/td>Non<\/td><\/tr>
Film PA (composant) (Polyamide)<\/td>V<\/td>V<\/td>V<\/td>V<\/td>V<\/td><\/tr>
Film PE (composant) (Polyéthylène)<\/td>Non<\/td>V<\/td>V<\/td>V<\/td>Non<\/td><\/tr>
Film PP (composant) (Polypropylène)<\/td>V<\/td>V<\/td>Non<\/td>Non<\/td>Non<\/td><\/tr>
Film PET (composant) (Polyéthylène Téréphtalate)<\/td>V<\/td>V<\/td>V<\/td>V<\/td>V<\/td><\/tr>
Film PETG (PETG-Foam-, PETG-PE) (PET Glycol)<\/td>Non<\/td>V<\/td>voir spécifications des fournisseurs<\/td>V<\/td>Non<\/td><\/tr>
Film PS (polystyrène)<\/td>Non<\/td>V<\/td>voir spécifications des fournisseurs<\/td>V<\/td>Non<\/td><\/tr>
Film HIPS (polystyrène à fort impact)<\/td>Non<\/td>V<\/td>voir spécifications des fournisseurs<\/td>V<\/td>Non<\/td><\/tr>
Film PC (polycarbonate)<\/td>V<\/td>V<\/td>voir spécifications des fournisseurs<\/td>V<\/td>V<\/td><\/tr>
Film PVC (polychlorure de vinyle)<\/td>Non<\/td>V<\/td>voir spécifications des fournisseurs<\/td>Non<\/td>Non<\/td><\/tr>
Film TPU (Polyuréthane thermoplastique)<\/td>Non<\/td>V<\/td>voir spécifications des fournisseurs<\/td>V<\/td>V<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n

<\/p>\n","protected":false},"excerpt":{"rendered":"

EO\/FORM (at least a part of the packaging needs to be permeable to 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Introduction The compatibility between sterile barrier systems (SBS) and sterilization processes is a critical engineering consideration in medical device packaging design. Inappropriate material-process combinations may lead to insufficient sterilant penetration, material degradation, or loss of microbial barrier integrity. 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Optimal material compatibility (Low temp). \"Product can be sterilized in its sealed final packaging.\" Simple operation and monitoring. Broad microbicidal activity. Low temperature. Sterility assurance and therapeutic effect. 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Equipment Design & Maintenance Standards 1.1 Design Documentation Detailed written descriptions (PFDs, P&IDs) must be provided in the initial\u2026","rel":"","context":"Similar post","block_context":{"text":"Similar post","link":""},"img":{"alt_text":"","src":"https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2026\/03\/eto-sterilizer-1.webp?resize=350%2C200&ssl=1","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2026\/03\/eto-sterilizer-1.webp?resize=350%2C200&ssl=1 1x, https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2026\/03\/eto-sterilizer-1.webp?resize=525%2C300&ssl=1 1.5x, https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2026\/03\/eto-sterilizer-1.webp?resize=700%2C400&ssl=1 2x, https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2026\/03\/eto-sterilizer-1.webp?resize=1050%2C600&ssl=1 3x, https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2026\/03\/eto-sterilizer-1.webp?resize=1400%2C800&ssl=1 4x"},"classes":[]},{"id":2224,"url":"https:\/\/zjbocon.com\/?p=2224","url_meta":{"origin":8915,"position":3},"title":"Factors Affecting the EO Gas Sterilization Process","author":"Bocon Technical Team","date":"2024-11-22","format":false,"excerpt":"Within a certain range of gas concentration, the higher the concentration, the better theEO Gas Sterilization effect; beyond 1000 mg\/L, the improvement in sterilization effect is not significant.","rel":"","context":"In "ETO STERILIZER"","block_context":{"text":"ETO STERILIZER","link":"https:\/\/zjbocon.com\/?cat=133124"},"img":{"alt_text":"","src":"https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2025\/09\/ethylene-oxide-sterilization-10-scaled.webp?resize=350%2C200&ssl=1","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2025\/09\/ethylene-oxide-sterilization-10-scaled.webp?resize=350%2C200&ssl=1 1x, https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2025\/09\/ethylene-oxide-sterilization-10-scaled.webp?resize=525%2C300&ssl=1 1.5x, https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2025\/09\/ethylene-oxide-sterilization-10-scaled.webp?resize=700%2C400&ssl=1 2x, https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2025\/09\/ethylene-oxide-sterilization-10-scaled.webp?resize=1050%2C600&ssl=1 3x, https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2025\/09\/ethylene-oxide-sterilization-10-scaled.webp?resize=1400%2C800&ssl=1 4x"},"classes":[]},{"id":2076,"url":"https:\/\/zjbocon.com\/?p=2076","url_meta":{"origin":8915,"position":4},"title":"PQ in Ethylene oxide sterilization chamber","author":"Bocon Technical Team","date":"2024-10-31","format":false,"excerpt":"PQ is the stage of validation that uses Ethylene oxide sterilization chamber to demonstrate that the Ethylene oxide sterilization equipment consistently operates in accordance with predetermined acceptance criteria and the process yields a product that is sterile and meets the specified requirements.","rel":"","context":"In "ETO STERILIZER"","block_context":{"text":"ETO STERILIZER","link":"https:\/\/zjbocon.com\/?cat=133124"},"img":{"alt_text":"","src":"https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2025\/09\/eto-sterilizer-1.webp?resize=350%2C200&ssl=1","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2025\/09\/eto-sterilizer-1.webp?resize=350%2C200&ssl=1 1x, https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2025\/09\/eto-sterilizer-1.webp?resize=525%2C300&ssl=1 1.5x, https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2025\/09\/eto-sterilizer-1.webp?resize=700%2C400&ssl=1 2x, https:\/\/i0.wp.com\/zjbocon.com\/wp-content\/uploads\/2025\/09\/eto-sterilizer-1.webp?resize=1050%2C600&ssl=1 3x"},"classes":[]},{"id":9625,"url":"https:\/\/zjbocon.com\/?p=9625","url_meta":{"origin":8915,"position":5},"title":"Factors Influencing Product Residuals","author":"Bocon Technical Team","date":"2026-05-06","format":false,"excerpt":"Explore technical factors influencing product residuals in EO sterilization. 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