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Diamond ABS 3500M
丙烯腈丁二烯苯乙烯
Network Polymers, Inc.
Technical Data
总体
材料状态 • 已商用：当前有效
资料 1 • Technical Datasheet
搜索 UL 黄卡 • Network Polymers, Inc.
• Diamond ABS
供货地区 • 北美洲
性能特点 • 中等抗撞击性
用途 • 医疗/护理领域的应用
机构评级 • EC 1907/2006 (REACH) • EU 2002/96/EC
RoHS 合规性 • RoHS 合规
UL 档案号 • E150937
外观 • 可用颜色
形式 • 颗粒料
加工方法 • 注射成型
物理性能 额定值单位制 测试方法
比重 1.04g/cm³ ASTM D792
熔流率 3 ASTM D1238
200°C/5.0 kg 2.9g/10 min
230°C/3.8 kg 8.5g/10 min
收缩率 - 流动 0.40 到 0.60% ASTM D955
机械性能 额定值单位制 测试方法
抗张强度 4 ASTM D638
屈服 43.2MPa
断裂 34.9MPa
伸长率 4 ASTM D638
屈服 2.4%
断裂 43%
弯曲模量 - 正切 5 2350MPa ASTM D790
冲击性能 额定值单位制 测试方法
悬壁梁缺口冲击强度 (23°C, 3.18 mm) 190J/m ASTM D256
硬度 额定值单位制 测试方法
洛氏硬度 (R 计秤) 108 ASTM D785
热性能 额定值单位制 测试方法
热变形温度 (1.8 MPa, 未退火, 3.18 mm) 77.2°C ASTM D648
维卡软化温度 107°C ASTM D1525 6
可燃性 额定值单位制 测试方法
UL 阻燃等级 (1.50 mm) HB UL 94
补充信息
MEDICAL BIOCOMPATIBILITY INFORMATION: All medical grade DIAMOND POLYMERS ABS resins (hereinafter "Product(s)'') meet the requirements of the USP CLASS VI. Only these PRODUCTS may be considered candidates for applications requiring biocompatibility. MANUFACTURER'S RESPONSIBILITY: It is the responsibility of the medical device, biological product or pharmaceutical
manufacturer ("Manufacturer") to determine the suitability of all component parts and raw materials, including any DIAMOND POLYMERS Product, used in its final product in order to ensure safety and compliance with FDA requirements. This determination must include, as applicable, testing for suitability as any non-implantable device and suitability for contact with and/or storage of human tissue and liquids including, without limitation, medication, blood or other bodily fluids and under no circumstances may any
DIAMOND POLYMERS Product be used in any implant applications (cosmetic, reconstructive or reproductive). The suitability of a DIAMOND POLYMERS product in a given end-use environment is dependent upon various conditions including, without limitation, chemical compatibility, temperature, part design, sterilization method, residual stresses or external loads. It is the responsibility of the
Manufacturer to evaluate its final device under actual end-use requirements and to adequately advise and warn purchasers and users thereof. Single-use medical devices made from a DIAMOND POLYMERS product are not suitable for multiple uses. If the medical device is designed for multiple uses, it is the responsibility of the Manufacturer to determine the appropriate number of permissible uses
Diamond ABS 3500M
丙烯腈丁二烯苯乙烯
Network Polymers, Inc.
by evaluating the device under actual sterilization and end-use conditions and to adequately advise and warn purchasers and users thereof.
STERILIZATION INFORMATION: The sterilization method and the number of sterilization cycles a medical device made from a DIAMOND POLYMERS Product can withstand will vary depending upon type/grade of product, part design, processing parameters, sterilization temperature, chemical environment and any other end-use application demands or requirements. Therefore, the MANUFACTURER must evaluate each device to determine the sterilization method and the number of permissible sterilization cycles appropriate for actual end-use requirements and most adequately advise and warn purchasers and users thereof.
The end use device produced by the manufacturer may be tested according to the ISO 10993 requirements. This testing is the responsibility of the device manufacturer. DIAMOND POLYMERS has elected to qualify their products for these applications by testing to USP Class VI requirements.
注射 额定值单位制
干燥温度 80.0 到 85.0°C
干燥时间 2.0 到 4.0hr
建议的最大水分含量 0.10%
螺筒后部温度 190 到 250°C
螺筒中部温度 190 到 250°C
螺筒前部温度 190 到 250°C
模具温度 40.0 到 80.0°C
注射速度 中等偏快
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