# AESCULAP SAS

FEI: 3001354499
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: Aesculap AG (#8010193)

Address: BOULEVARD DU MARECHAL JUIN, BP 2024, CHAUMONT Grand Est, 52901, FR

Mandatory US Agent: Aesculap, Inc.

## Products

Total registered: 1
Top product codes: HWA
Regulation §: 888.4540

Proprietary names: AESCULAP

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223001354499%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3001354499