GelMA, 250g Bloom, 75-85%, Medical Grade

GelMA-MH23

Background

Vita Spire has developed a series of bioinks for biomedical applications, featuring stricter quality control standards than reagent-grade products. All products are manufactured under ISO 13485:2016, with strict monitoring of residual Methyl methacrylate content. To meet biomedical requirements, all products undergo endotoxin removal processes, and microbial levels are tightly controlled to ensure product safety and consistency.

Technical Specifications

Features
White powder
Impurities
MAA Residue: <1000µg/g Endotoxin: <0.5EU/mg Total Aerobic Microbial Count: <100CFU/g Mold & Yeast: <10CFU/g
Morphology & Appearance
White powder