Product Description: Ultraform® N 2320 003 PRO AT is an unfilled injection molding POM grade, which supports customers in product development for the medical technology market. This grade complies with US Pharmacopeia: 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 and Food Contact: Ultraform® PRO is in compliance with multiple regional food contact regulations, especially for Europe and United States. This material can be used for functional parts in devices such as insulin pens or powder inhalers as well as plug in connectors or medical device handles. Availability: North America Features: Food Contact Acceptable Use: Medical/Healthcare Applications Agency Ratings: DMF; EC 1907/2006 (REACH); FDA Food Contact; ISO 10993 Part 5; USP Class VI RoSH Compliance: RoSH Compliant Processing Method: Injection Molding Information provided by BASF Corporation |