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Medical blister box
Negotiable
  • 付款方式:
    银联转账/支付宝/微信
  • 交货时间:
    15 days
  • 物流:
    邮政EMS
  • 最低订购:
    200
  • 港口:
    上海市

Medical Blister Packaging Introduction

Product Overview

Our medical blister packaging is engineered as a sterile barrier system for medical devices. Manufactured in strict compliance with ISO 11607 and EN 868 standards, these thermoformed trays offer robust physical protection and an effective microbial barrier for Class II and Class III medical devices. Ideal for surgical instruments, catheters, syringes, and high-value consumables, our packaging ensures product integrity throughout sterilization and transit.

 

Key Features

Superior Microbial Barrier: Made from high-grade pharmaceutical films, our blister trays feature excellent bacterial resistance. They provide a seamless, channel-free heat seal with Tyvek® or medical-grade coated paper, meeting rigorous requirements for sterile barrier maintenance.

 

Versatile Material Options: We support a variety of high-clarity medical polymers, including PETG, APET, PVC, PS, and PP. Among these, PETG is preferred for high-end medical packaging due to its outstanding impact resistance, puncture resistance, and superior thermoforming capabilities.

 

Custom-Engineered Designs: We offer full custom mold design services tailored to specific device geometries. Features such as reinforced ribs and support partitions are integrated to enhance compression strength, preventing deformation and damage during handling and shipping.

 

Compatible with Multiple Sterilization Methods: Our packaging is compatible with Ethylene Oxide (EtO), Irradiation (Gamma/E-beam), and Low-Temperature Plasma sterilization. All materials are validated for aging and sterilization adaptability to ensure performance longevity.

 

Quality Assurance

Manufactured in ISO Class 8 (10,000-grade) cleanrooms, our operations strictly adhere to the ISO 13485 quality management system. We implement full-process quality control—from raw material biocompatibility verification to final product bioburden and particulate testing—guaranteeing compliance with global medical device regulations.

 


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