# AESCULAP AG

FEI: 3002806315
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: Aesculap AG (#8010193)

Address: AM AESCULAP PLATZ, TUTTLINGEN, DONAU Baden-Wurttemberg, D-78532, DE

Mandatory US Agent: Aesculap, Inc.

## Products

Total registered: 1
Top product codes: GWG
Regulation §: 882.1480


## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223002806315%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3002806315