FDA Device Establishments · JSON-LD · Markdown

CLERAD

FEI 3009518669 · Manufacture Medical Device for Another Party (Contract Manufacturer) Manufacture Medical Device · Status: Active

FEI Number3009518669
Owner / OperatorCLERAD (#10041828)
Address184-186 avenue Gustave Flaubert, Clermont-Ferrand Puy-de-Dome, 63000, FR
Mandatory US AgentMINVASIVE SURGICAL
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)IZD
Regulation § (21 CFR)892.1320
Proprietary namesKUBTEC GammaPRO; GAMMA SUP II

External sources

Source: openFDA. Public-domain (CC0).