FDA Device Establishments · JSON-LD · Markdown

NOVO NORDISK A/S

FEI 3003131673 · Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility · Status: Active

FEI Number3003131673
Owner / OperatorNOVO NORDISK INC. (#9027307)
AddressBRENNUM PARK, HILLEROED Hovedstaden, DK-3400, DK
Mandatory US AgentNOVO NORDISK INC.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)KZH
Regulation § (21 CFR)880.6920
Proprietary namesFLEXPRO PENMATE

External sources

Source: openFDA. Public-domain (CC0).