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Ultraform® W2320 003 PRO AT

Ultraform® W2320 003 PRO AT

Ultraform® W2320 003 PRO AT

POM(聚甲醛)

巴斯夫 (BASF)

产品描述

Very free-flowing, rapidly solidifying grade for use where processing is extremely difficult but mechanical properties are lower.

Ultraform® PRO offers a comprehensive service package, which supports customers in product development for the medical technology market. 

Ultraform® PRO complies with the basic requirements of Pharmacopoeia and Biocompatibility-Tests in Europe, United States and Japan respectively as specified below. However, the biocompatibility tests were recorded on tests specimens of Ultraform PRO to show compatibility and potential suitability of the material in general. The biocompatibility-tests and the other tests listed below are not part of any continuous production control. 

 

European Pharmacopoeia, Japanese Pharmacopoeia: 

The composition of the product complies with the basic requirements of the European Pharmacopoeia 8th Edition, Chap. 3.2.2. "Plastic Containers and Closures for Pharmaceutical Use" and with the basic requirements of the Japanese Pharmacopoeia,16th 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 (E-Mail: ultraplaste.infopoint@basf.com, Telefon: +49 621-60-78780, Fax: +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. 

 

Abbreviated designation according to ISO 1043-1: POM 

Designation according to ISO 29988-POM-K,,M-GNR,4-2

基本信息
原厂资料
物性表(英文)
产品特性
易成型
食品接触级
医疗级
法规认证
DMF(药品主控文件)
ISO10993(生物相容性)
USP Class VI(美国药典)
成型方式
注塑
技术参数
物理性能 值/单位 测试标准 测试条件

密度

1.41 g/cm³ ISO 1183

熔体体积流动速率(MVR)

190℃/2.16 kg

25 cm³/10min ISO 1133

收缩率

纵向(Flow)

2 % ISO 294-4

横向(Across Flow)

2.1 % ISO 294-4

吸水率

0.8 % ISO 62
equilibrium in water at 23°C

吸湿率

0.2 % ISO 62
equilibrium 23°C/50% r.h.
机械性能 值/单位 测试标准 测试条件

拉伸强度

屈服(yld)

65 Mpa ISO 527-1/-2
50 mm/min

拉伸延伸率

屈服(yld)

8 % ISO 527-1/-2
50 mm/min

标称断裂伸长率

24 % ISO 527-1/-2
50 mm/min

弯曲模量

2800 Mpa ISO 178

拉伸模量

2850 Mpa ISO 527-1/-2

拉伸蠕变模量

1000h

1350 Mpa ISO 899-1
strain ≤ 0.5%, 23°C
冲击性能 值/单位 测试标准 测试条件

简支梁缺口(Charpy Notched)

-30℃ (-22℉)

4 kJ/m² ISO 179/1eA

23℃ (73℉)

4.5 kJ/m² ISO 179/1eA

简支梁无缺口(Charpy Unnotched)

-30℃ (-22℉)

190 kJ/m² ISO 179/1eU

23℃ (73℉)

190 kJ/m² ISO 179/1eU

悬臂梁缺口(Izod Notched)

-30℃ (-22℉)

5 kJ/m² ISO 180/A

23℃ (73℉)

5 kJ/m² ISO 180/A
硬度性能 值/单位 测试标准 测试条件

球压硬度

145 Mpa ISO 2039-1
358 N and 30 s
热学性能 值/单位 测试标准 测试条件

热变形温度(HDT)

1.8 Mpa (264 psi)(18.6kg/cm²)

100 °C ISO 75-1/-2

线性膨胀系数(CLTE)

纵向(Flow)

110 E-6/K ISO 11359-1/-2
(23-55)°C

熔融温度(Tm)

166 °C ISO 11357-1/-3
DSC

短周期使用温度

100 °C -

加工温度

190~230 °C -
Injection moulding

模具温度

60~120 °C -
Injection moulding
燃烧性能 值/单位 测试标准 测试条件

UL 防火等级

HB

1.5 mm IEC 60695-11-10

FMVSS

+ pass FMVSS 302
thickness d ≥ 1mm

燃烧速率

100 mm/min ISO 3795
d < 1 mm
电学性能 值/单位 测试标准 测试条件

体积电阻率

1.0E+11 Ohm-m IEC 62631-3-1

表面电阻率

1.0E+13 Ohm IEC 62631-3-2

介电常数(DK)

1MHz

3.8 - IEC 62631-2-1

耗散因数(DF)

1MHz

50 E-4 IEC 62631-2-1

相比漏电起痕指数(CTI )

溶液A

600 V IEC 60112
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