# KERI MEDICAL

FEI: 3024706750
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: Keri Medical (#10085771)

Address: Chemin du Pre-Fleuri 5, Plan-les-Ouates Geneve, 1228, CH

Mandatory US Agent: Nilson Law Group

## Products

Total registered: 1
Top product codes: FSM
Regulation §: 878.4800

Proprietary names: Kirschner wire Tube

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223024706750%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3024706750