# OEM DEVELOPMENT

FEI: 3031600052
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner/operator: OEM Developement (#10091097)

Address: 39 BVD de la romanerie, SAINT BARTHELEMY D ANJOU Maine-et-Loire, 49124, FR

Mandatory US Agent: Registrar Corp

## Products

Total registered: 1
Top product codes: KDN
Regulation §: 876.5880

Proprietary names: RM4 KIDNEY PERFUSION SYSTEM

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223031600052%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3031600052