FDA Device Establishments · JSON-LD · Markdown

AESCULAP SAS

FEI 3001354499 · Manufacture Medical Device · Status: Active

FEI Number3001354499
Owner / OperatorAesculap AG (#8010193)
AddressBOULEVARD DU MARECHAL JUIN, BP 2024, CHAUMONT Grand Est, 52901, FR
Mandatory US AgentAesculap, Inc.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)HWA
Regulation § (21 CFR)888.4540
Proprietary namesAESCULAP

External sources

Source: openFDA. Public-domain (CC0).