Vitaflow Capital Bundle w/ Cart Brand Name or Equal RFP
Open
Aug 14, 2026
Closes
Aug 26, 2026
To be considered an acceptable "equal" product, an offered ECMO system must meet or exceed the following salient characteristics. FDA clearance / regulatory classification: Class II device cleared under 21 CFR 870.4100 (Extracorporeal Circuit and Accessories for Long-Term Respiratory/Cardiopulmonary Failure), or equivalent product code classification (e.g., QNR for pump/console, BYS for oxygenator). Indicated duration of use: Indicated for continuous ECMO support up to 48 hours. See attached file.
