FDA Device Establishments · JSON-LD · Markdown

PAUL HARTMANN S.A.

FEI 3009080375 · Manufacture Medical Device · Status: Active

FEI Number3009080375
Owner / OperatorPAUL HARTMANN AG (#8010690)
AddressP.I. Pla d en Boet II, Carrasco i Formiguera, 48, Mataro Barcelona, E-08302, ES
Mandatory US AgentHARTMANN USA
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)KGX
Regulation § (21 CFR)880.5240
Proprietary namesCosmopor Transparent Steril

External sources

Source: openFDA. Public-domain (CC0).