FDA Device Establishments · JSON-LD · Markdown

AESCULAP CHIFA SP. Z O.O.

FEI 3002315844 · Manufacture Medical Device · Status: Active

FEI Number3002315844
Owner / OperatorAESCULAP CHIFA SP. Z O. O. (#9007699)
AddressUL. TYSIACLECIA 14, NOWY TOMYSL Wielkopolskie, 64-300, PL
Mandatory US AgentAesculap, Inc.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)GEG
Regulation § (21 CFR)878.4800
Proprietary namesELEVATOR, SURGICAL, GENERAL & PLASTIC SURGERY

External sources

Source: openFDA. Public-domain (CC0).