Ultraform N2320 003 BK120是一種 （POM） 級。提供強度、剛度和硬度的理想組合。具有良好的回彈性和加工性能，適用于過熱蒸汽、等離子體和環氧乙烷滅菌。與其他超成型牌號相比，具有高結晶度和更高的粘度。具有高摩擦強度、高抗沖擊性、低摩擦、良好的抗磨性、低材料疲勞性、良好的耐化學性和耐水解性。可與 Ultradur 結合使用，用于生產具有附加功能的塑料部件。經注塑成型加工而成，適用于生產厚壁部件和制造高應力元件，例如胰島素筆、霧化裝置和干粉吸入器的功能部件，以及插入式連接器、手術器械手柄和其他由半成品制成的部件。符合歐盟藥典、美國藥典和 DIN EN ISO 10993-5。符合 FDA 和 REACH 規定（EC 法規第 1907/2006 號）。符合 RoHS 指令 2002/95/EC、CONEG（1994 年 1 月 1 日）和歐盟指令 94/62/EEC。

Ultraform N2320 003 BK120 is a polyoxymethylene; polyacetal (POM) grade. Provides an ideal combination of strength, stiffness and hardness. Offers good resilience, processability and is suitable for sterilization with superheated steam, plasma and ethylene oxide. Possesses high crystallinity and has higher viscosity as compared to other Ultraform grades. Exhibits high tribological strength, high impact resistance, low friction, good abrasion resistance, low material fatigue, excellent chemical and hydrolysis resistance. Can be combined with Ultradur for producing plastic parts with additional features. Processed by injection molding and suited for the production of thick-walled components and manufacture of highly stressed elements such as functional parts in insulin pens, atomizing devices and dry-powder inhalers as well as for plug-in connectors, handles of surgical instruments and other components in made from semi-finished parts. Is in accordance with EU Pharmacopeia, US Pharmacopeia and DIN EN ISO 10993-5. Complies with FDA and REACH stipulations (EC Regulation No. 1907/2006). Adheres to RoHS Directive 2002/95/EC, CONEG (dated January 1, 1994) and EU Directive 94/62/EEC.