FDA Device Establishments · JSON-LD · Markdown

AESCULAP AG

FEI 3002806315 · Manufacture Medical Device · Status: Active

FEI Number3002806315
Owner / OperatorAesculap AG (#8010193)
AddressAM AESCULAP PLATZ, TUTTLINGEN, DONAU Baden-Wurttemberg, D-78532, DE
Mandatory US AgentAesculap, Inc.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)GWG
Regulation § (21 CFR)882.1480

External sources

Source: openFDA. Public-domain (CC0).