FDA Device Establishments · JSON-LD · Markdown

MEDI.PLAN GMBH & CO. KG

FEI 3033536319 · Export Device to the United States But Perform No Other Operation on Device · Status: Active

FEI Number3033536319
Owner / OperatorMEDI.PLAN GmbH & Co. KG (#10091549)
AddressHofkerstrabe 22, Dortmund North Rhine-Westphalia, 44149, DE
Mandatory US AgentCapote Law Firm
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)FMI
Regulation § (21 CFR)880.5570
Proprietary namesBD SAFETYGLIDE NEEDLE 25GX1" PACK 50; BD SAFETYGLIDE NEEDLE 21GX1" PACK 50; BD SAFETYGLIDE NEEDLE 23GX1" PACK 50; BD SAFETYGLIDE NEEDLE 25GX1-1/2 PACK 50; BD SAFETYGLIDE NEEDLE 25GX5/8" PACK 50; BD SAFETYGLIDE NEEDLE 18GX1-1/2 PACK 50

External sources

Source: openFDA. Public-domain (CC0).