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Diamond ABS 1000M
丙烯腈丁二烯苯乙烯
Network Polymers, Inc.
Technical Data
總體
材料狀態 • 已商用：當前有效
資料 1 • Technical Datasheet
搜索 UL 黃卡 • Network Polymers, Inc.
• Diamond ABS
供貨地區 • 北美洲
性能特點 • 光澤，高
用途 • 醫療/護理領域的應用
機構評級 • EC 1907/2006 (REACH) • EU 2002/96/EC
RoHS 合規性 • RoHS 合規
UL 檔案號美國 • E150937
外觀 • 可用顏色
形式 • 顆粒料
加工方法 • 注射成型
物理性能 額定值單位制 測試方法
比重 1.06g/cm³ ASTM D792
熔流率 ASTM D1238
200°C/5.0 kg 3.5g/10 min
230°C/3.8 kg 3 13g/10 min
收縮率 - 流動 0.40 到 0.60% ASTM D955
機械性能 額定值單位制 測試方法
抗張強度 4 (屈服) 51.7MPa ASTM D638
彎曲模量 - 正切 5 2540MPa ASTM D790
沖擊性能 額定值單位制 測試方法
懸壁梁缺口沖擊強度 (23°C, 3.18 mm) 80J/m ASTM D256
硬度 額定值單位制 測試方法
洛氏硬度 (R 計秤) 115 ASTM D785
熱性能 額定值單位制 測試方法
熱變形溫度 ASTM D648
1.8 MPa, 未退火, 3.18 mm 78.0°C
1.8 MPa, 退火, 3.18 mm 92.8°C
維卡軟化溫度 104°C ASTM D1525
可燃性 額定值單位制 測試方法
UL 阻燃等級 (1.59 mm) HB UL 94
補充信息
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 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,
Diamond ABS 1000M
丙烯腈丁二烯苯乙烯
Network Polymers, Inc.
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 額定值單位制
干燥溫度 80.0 到 85.0°C
干燥時間 2.0 到 4.0hr
建議的最大水分含量 0.10%
螺筒后部溫度 190 到 250°C
螺筒中部溫度 190 到 250°C
螺筒前部溫度 190 到 250°C
模具溫度 40.0 到 80.0°C
注塑溫度 48.3 到 75.8MPa
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