FDA Device Establishments · JSON-LD · Markdown

REBOTEC REHABILITATIONSMITTEL GMBH

FEI 3006481901 · Export Device to the United States But Perform No Other Operation on Device · Status: Active

FEI Number3006481901
Owner / OperatorRebotec Rehabilitationsmittel GmbH (#10051753)
AddressArtlandstrabe 57, Quakenbruck Lower Saxony, 49610, DE
Mandatory US AgentTR GROUP, INC.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)INN
Regulation § (21 CFR)890.3100
Proprietary namesPluto2 Rollator; Pluto1 Rollator; Fox Rollator; Fixi Rollator; Walk-On Small; Walk-On Medium

External sources

Source: openFDA. Public-domain (CC0).