FDA食品级ABS/ABS 4012M/FDA食品接触的合规性/抗撞击性高/医疗/护理领域的应用/吹塑成型

FDA食品级ABS,FDA食品级丙烯腈丁二烯苯乙烯,ABS FDA食品接触的合规性 ABS Diamond ABS 4012M是东莞市双帮塑胶原料有限公司常年销售的塑料，因为塑料价格行情每天都有新变化前天的报价不等于今天的报价。本公司销售的所有原料保证是原厂原包,随料可以提供生产厂商提供的物性表、SGS报告，COA原料出厂报告,REACH报告,SVHC报告,UL黄卡,提供原料注塑加工工程中可能出现的各种异常现象解决方法，塑料牌号太多，本网站没有提供的本公司也有代理，详情请咨询本公司相关业务人员0769-87795123

13549213581 肖生

FDA食品接触的合规性, 抗撞击性高, 医疗/护理领域的应用, 吹塑成型

Diamond ABS 4012M

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 • 抗撞击性，高

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

外观 • 可用颜色

形式 • 颗粒料

加工方法 • 吹塑成型

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 (220°C/10.0 kg) 1.3g/10 min ASTM D1238

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 (屈服) 39.0MPa ASTM D638

弯曲模量 - 正切 5 1870MPa 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) 340J/m ASTM D256

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) 84.4°C ASTM D648

维卡软化温度 115°C ASTM D1525 6

光学性能额定值单位制测试方法

Gardner光泽度 (60°) 97 ASTM D523

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 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

Diamond ABS 4012M

丙烯腈丁二烯苯乙烯

Network Polymers, Inc.

注射额定值单位制

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

13549213581 肖生