聚甲醛塑料,俗稱賽鋼,為結晶性熱可塑性塑料,具明顯熔點165~175℃,性質zui接近金屬。
產品說明 | |
Preliminary Datasheet Rapidly solidifying standard grade for injection molding. Ultraform® PRO offers a comprehensive service package, which supports customers in product development for the medical technology market. Ultraform® PRO is in compliance with Pharmacopoeia and Biocompatibility-Tests in Europe, United States and Japan as specified below. However, the biocompatibility tests were recorded on tests specimens of Ultraform PRO to show compatibility of the material in general. The biocompatibility-tests listed below are not part of any continuous production control. European Pharmacopoeia, Japanese Pharmacopoeia: The composition of the product complies with the requirements of the European Pharmacopoeia 7th Edition, Chap. 3.2.2. "Plastic Containers and Closures for Pharmaceutical Use" and with the requirements of the Japanese Pharmacopoeia, 15th Edition, General Information, "17. Plastic Containers for Pharmaceutical Products". However, suitability for the end application concerned including observation of given limitations and toxicological thresholds have to be ensured on the final article by the producer. US Pharmacopoeia: Biological Reactivity Tests, USP Plastic Class VI (USP VI) ISO 10993-5: Biological Evaluation of Medical Devices Part 5: Test for Cytotoxicity DMF: A Drug Master File (DMF) has been registered at FDA for Ultraform® PRO. Food Contact: Ultraform® PRO is in compliance with multiple regional food contact regulations, especially for Europe and United States. Additional compliances may also be available. Please contact your local representative or the Ultraplaste Infopoint (: ultraplaste.infopoint@basf.com, efon: +49 621-60-78780, +49 621-60-78730). For notice: However, BASF has not designed or tested its plastics with respect to all of the special requirements related to their use in medical devices (defined in risk classes I to III according to the European and US Medical Device legislation) and pharmaceutical applications. Therefore BASF makes no warranties, express or implied, concerning the suitability of any BASF plastics for use in any medical device and pharmaceutical applications. | |
總體 | |
材料狀態 | 已商用:當前有效 |
資料 1 | Processing - Injection Molding Cooling Times (English)Technical Datasheet (English) |
搜索 UL 黃卡 | BASF CorporationUltraform® |
供貨地區 | 北美洲歐洲亞太地區 |
性能特點 | 生物兼容性 |
用途 | 藥物醫療/護理領域的應用 |
機構評級 | DMF 未評級EC 1907/2006 (REACH)EP Monograph 3.2.2ISO 10993 Part 5USP 第VI類 |
RoHS 合規性 | RoHS 合規 |
形式 | 顆粒 |
加工方法 | 注射成型 |
樹脂ID (ISO 1043) | POM |
物理性能 | 額定值 | 單位制 | 測試方法 |
密度 | 1.40 | g/cm3 | ISO 1183 |
溶化體積流率(MVR) (190°C/2.16 kg) | 0.458 | in3/10min | ISO 1133 |
吸水率 | ISO 62 | ||
飽和, 73°F | 0.80 | % | |
平衡, 73°F, 50% RH | 0.20 | % | |
硬度 | 額定值 | 單位制 | 測試方法 |
球壓硬度 (H 358/30) | 21000 | psi | ISO 2039-1 |
機械性能 | 額定值 | 單位制 | 測試方法 |
拉伸模量 (73°F) | 392000 | psi | ISO 527-2 |
拉伸應力 (屈服, 73°F) | 9430 | psi | ISO 527-2/50 |
拉伸應變 (屈服, 73°F) | 9.4 | % | ISO 527-2/50 |
斷張率 (73°F) | 27 | % | ISO 527-2/50 |
拉伸蠕變模量 2 (1000 hr) | 203000 | psi | ISO 899-1 |
沖擊性能 | 額定值 | 單位制 | 測試方法 |
簡支梁缺口沖擊強度 | ISO 179/1eA | ||
-22°F | 2.6 | ft·lb/in2 | |
73°F | 2.9 | ft·lb/in2 | |
簡支梁缺口沖擊強度 | ISO 179/1eU | ||
-22°F | 90 | ft·lb/in2 | |
73°F | 100 | ft·lb/in2 |
熱性能 | 額定值 | 單位制 | 測試方法 |
熱變形溫度 (264 psi, 未退火) | 212 | °F | ISO 75-2/A |
熔融溫度 | 333 | °F | ISO 11357-3 |
線形膨脹系數 - 流動 (73 到 131°F) | 0.000061 | in/in/°F | ISO 11359-2 |
zui高使用溫度 - Short Cycle Operation | 212 | °F |
電氣性能 | 額定值 | 單位制 | 測試方法 |
表面電阻率 | 1.0E+13 | ohm | IEC 60093 |
體積電阻率 | 1.0E+15 | ohm·cm | IEC 60093 |
相對電容率 (73°F, 1 MHz) | 3.80 | IEC 60250 | |
耗散因數 (73°F, 1 MHz) | 0.0050 | IEC 60250 | |
漏電起痕指數 (解決方案 A) | 600 | V | IEC 60112 |
可燃性 | 額定值 | 單位制 | 測試方法 |
UL 阻燃等級 (0.0630 in) | HB | UL 94 |
補充信息 | 額定值 | 測試方法 | |
Automotive Materials (> 39.4 mil) | + | FMVSS 302 | |
ISO Type | POM-K, M-GNR, 03-002 | ISO 9988-1 | |
Polymer Abbreviation | POM |
注射 | 額定值 | 單位制 | |
加工(熔體)溫度 | 374 到 446 | °F | |
模具溫度 | 140 到 248 | °F |
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傳真號碼:86-
地址:廣東 東莞市
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