FDA Device Establishments · JSON-LD · Markdown

PERIVISION S.A.

FEI 3030491936 · Manufacture Medical Device Export Device to the United States But Perform No Other Operation on Device · Status: Active

FEI Number3030491936
Owner / OperatorPerivision S.A. (#10090044)
AddressRoute de la Corniche 3, Epalinges Vaud, 1066, CH
Mandatory US AgentRegistrar Corp
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)HPT
Regulation § (21 CFR)886.1605
Proprietary namesVisionOne

External sources

Source: openFDA. Public-domain (CC0).