补充描述:
This Clamp is manufactured under a dual ISO 9001 and ISO 13485 quality system, meeting USP <88> Class VI biological safety requirements, USP <87> in vitro non-toxicity testing, bacterial endotoxin limits equivalent to Water for Injection (≤0.25 EU/mL), and particulate matter specifications aligned with the Chinese Pharmacopoeia (2020 edition) and USP <788>. It is supplied — rather than directly manufactured — by Shenzhen ActiveCell Technology Co., Ltd., with free samples available, and sold across North America, Central/South America, Western and Eastern Europe, Australasia, Asia, the Middle East and Africa.
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