# MANUFACTURE VENDOME

FEI: 3042244330
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device; Manufacture Medical Device
Owner/operator: Manufacture Vendome (#10094101)

Address: 19 Rue de Mons, VENDOME Loir-et-Cher, 41100, FR

Mandatory US Agent: kapo optik

## Products

Total registered: 1
Top product codes: HQZ
Regulation §: 886.5842


## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223042244330%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3042244330