HyClone WFI, USP Grade, (6 x 1000mL)
BioProcess Applications Cell Culture Media & Purification Buffers
Pharmaceutical Manufacturing
Medical Device Processing and Testing
Manufactured under cGMP and ISO 13485 guidelines in a FDA registered facility.
Complies with the United States Pharmacopoeia (USP) monograph for water for injection packaged in bulk for commercial use elsewhere.
Nitrosamine Impurity Free
Our Terminally Distilled Water for Injection (WFI) is is a sterile, nonpyrogenic preparation which contains no bacteriostat, antimicrobial agent or added buffer. It complies with both United States Pharmacopoeia (USP) testing monograph for water for injection packaged in bulk for commercial use elsewhere.