FDA Device Establishments · JSON-LD · Markdown

OEM DEVELOPMENT

FEI 3031600052 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active

FEI Number3031600052
Owner / OperatorOEM Developement (#10091097)
Address39 BVD de la romanerie, SAINT BARTHELEMY D ANJOU Maine-et-Loire, 49124, FR
Mandatory US AgentRegistrar Corp
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)KDN
Regulation § (21 CFR)876.5880
Proprietary namesRM4 KIDNEY PERFUSION SYSTEM

External sources

Source: openFDA. Public-domain (CC0).