FDA Device Establishments · JSON-LD · Markdown

PERIMED AB

FEI 3003244961 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active

FEI Number3003244961
Owner / OperatorPERIMED AB (#8030885)
AddressDATAVAGEN 9 A, JARFALLA Stockholm, 17543, SE
Mandatory US AgentPerimed Inc
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)DPT
Regulation § (21 CFR)870.2120
Proprietary namesPeriCam PSI HR; PeriCam PSI System; PeriCam PSI NR; PeriCam PSI

External sources

Source: openFDA. Public-domain (CC0).