# Dilon Technologies France SAS

FEI: 3007702492
Status: Active
Establishment types: Repack or Relabel Medical Device; Manufacture Medical Device
Owner/operator: DILON TECHNOLOGIES Inc (#9035906)

Address: 8 Allee Irene Joliot Curie, St Priest Rhone, 69800, FR

Mandatory US Agent: Dilon Technologies

## Products

Total registered: 1
Top product codes: PMX
Regulation §: 878.4490

Proprietary names: HEMOBLAST™ Bellows

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223007702492%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3007702492