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• 已商用：當前有效

•  Technical Datasheet

•  普立萬公司

•  Versaflex™

• 北美洲

• 非洲和中東

• 好的消毒性

• 良好的成型性能

• 包覆成型

• 插頭

• ISO 10993 Part 4

• RoHS 合規

• 自然色

• 粒子

• 注射成型

醫療級TPE,TPE 32A,醫療護理用品, ISO 10993 Part 5, USP 第 VI 類 2

 

Versaflex™ HC 2110-35N

熱塑性彈性體

 

普立萬公司

 

Technical Data

 

產品說明

Versaflex™ HC 2110-35N is a thermoplastic elastomer developed as an alternative to traditional isoprene rubber solutions for infusion stoppers & septums that require multiple needle penetration with good resealing performance. Versaflex™ HC 2110-35N addresses needs such as low piercing force and good spike retention.

- Overmolds to PP and PE 

- Approved to ISO 10993-4 & -5 

- Approved to USP VI 

- Approved to USP 381: Elastomeric closures for injection. 

 

總覽

 

材料狀態

 

 

資料 1

 

搜索 UL 黃卡

 

供貨地區

 

特性

 

用途

 

機構評級 RoHS 合規性 外觀 形式 加工方法

 

 

 

 

• 拉丁美洲

• 亞太地區

• 良好的加工穩定性 • 良好的著色性

• 良好的流動性 • 脫模性能良好

• 密封件 • 膜

• 密封裝置 • 醫療/護理用品

• ISO 10993 Part 5 • USP 第 VI 類 2

 

 

物理性能 額定值(英制) 額定值(公制) 測試方法

密度 / 比重 0.890 0.888g/cm³ ASTM D792

彈性體 額定值(英制) 額定值(公制) 測試方法

拉伸應力 4, 5 (100%應變, 73°F (23°C)) 100psi 0.689MPa ASTM D412

抗張強度 4, 5 (斷裂, 73°F (23°C)) 452psi 3.12MPa ASTM D412

伸長率 4, 5 (斷裂, 73°F (23°C)) 750% 750% ASTM D412

撕裂強度 97.1lbf/in 17.0kN/m ISO 34-1

壓縮永久變形 ISO 815

73°F (23°C), 72 hr 19% 19%

158°F (70°C), 22 hr 33% 33%

212°F (100°C), 22 hr 47% 47%

硬度 額定值(英制) 額定值(公制) 測試方法

肖氏硬度 (邵氏 A, 10 秒) 32 32 ASTM D2240

充模分析 額定值(英制) 額定值(公制) 測試方法

表觀粘度 (392°F (200°C), 11200 sec^-1) 10.7Pa·s 10.7Pa·s ASTM D3835

注射 額定值(英制) 額定值(公制)

建議的最大回制料比例 20% 20%

料筒后部溫度 360 到 380°F 182 到 193°C

料筒中部溫度 430 到 460°F 221 到 238°C

料筒前部溫度 460 到 480°F 238 到 249°C

射嘴溫度 460 到 480°F 238 到 249°C

加工（熔體）溫度 450 到 480°F 232 到 249°C

模具溫度 60 到 90°F 16 到 32°C

背壓 0.00 到 80.0psi 0.00 到 0.552MPa

螺桿轉速 80 到 200rpm 80 到 200rpm

 

Versaflex™ HC 2110-35N

熱塑性彈性體

普立萬公司

 

注射說明

Color concentrates with polypropylene (PP), ethylene vinyl acetate (EVA), or polyethylene (PE) carriers are most suitable for coloring Versaflex™ HC 2110-35N. Improved color dispersion can be achieved by using higher melt flow concentrates (with a melt flow from 25 - 40 g/10 min). Typical loadings for color concentrates are 1% to 5% by weight. Liquid color can be used, but mineral oil based carriers may have a significant effect on the final hardness value. Concentrates based on PVC should not be used. A high color match consistency can be obtained by using precolored compounds available from GLS. The final determination of color concentrate suitability should be determined by customer trials.

 

Purge thoroughly before and after use of this product with a low flow (0.5 - 2.5 MFR) polyethylene (PE) or polypropylene (PP).

 

Regrind levels up to 20% can be used with Versaflex™ HC 2110-35N with minimal property loss, provided that the regrind is free of contamination. To minimize losses during molding, the melt temperature should remain as low as possible. The final determination of regrind effectiveness should be determined by the customer.

 

Versaflex™ HC 2110-35N has excellent melt stability. Maximum residence times may vary, depending on the size of the barrel. Generally, the barrel should be emptied if it is idle for periods of 8 - 10 minutes or longer.

 

Drying is not Required

 

Injection Speed: 1 to 3 in/sec

1st Stage - Boost Pressure: 800 to 1200 psi 2nd Stage - Hold Pressure: 40-70% of Boost Hold Time (Thick Part): 2 to 5 sec

Hold Time (Thin Part): 1 to 4 sec

 

備注

1 通過這些鏈接您能夠訪問供應商資料。我們盡量保證及時更新資料；不過您可以從供應商處了解最新資料。

2 Please contact PolyOne GLS Thermoplastic Elastomers for a complete copy of the GLS Healthcare Policy.

 

1. The Customer must notify GLS of any FDA Class I and/or European Union Class I medical devices for each specific product and application. 2. The Customer shall not knowingly manufacture, use, sell or otherwise supply, directly or indirectly products or compounds made from GLS products in any of the following without prior written approval by GLS for each specific product or application:

a. Cosmetics

b. Drugs and other Pharmaceuticals

 

c. Temporary or permanent implantation in the human body, regardless of the intended duration of implantation d. Class II and Class III Medical Devices as defined in 21 CFR 860.3 ("Medical Devices")

 

e. Class IIa, IIb and III as defined in Directive 93/42/EEC 3 一般屬性：這些不能被視為規格。

4 C 模具

 

5 2 小時

 

 

 

 

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