FDA Device Establishments · JSON-LD · Markdown

LUMINOAH

FEI 3046434077 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active

FEI Number3046434077
Owner / OperatorLuminoah (#10096019)
Address1 Morton Dr Ste 100, Charlottesville, VA, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)LZH
Regulation § (21 CFR)880.5725
Proprietary namesLuminoah Flow Enteral Nutrition Delivery System; Luminoah Flow Enteral Pump; Luminoah Flow Enteral System; Luminoah Flow Enteral Feeding Pump; Luminoah Flow Enteral Nutrition System

External sources

Source: openFDA. Public-domain (CC0).