FDA Device Establishments · JSON-LD · Markdown

Cardioline S.P.A.

FEI 3009735945 · Manufacture Medical Device · Status: Active

FEI Number3009735945
Owner / OperatorCARDIOLINE SPA (#10041348)
AddressVia Linz 151, TRENTO, 38121, IT
Mandatory US AgentQserve Group US Inc.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)DRG
Regulation § (21 CFR)870.2910
Proprietary namesPATIENT CABLE SNAP 10 WIRES IEC FOR HD+ ORANGE; PATIENT CABLE PLUG 10 WIRES AHA FOR HD+ ORANGE; PATIENT CABLE SNAP 10 WIRES AHA FOR HD+; HD+12

External sources

Source: openFDA. Public-domain (CC0).