# NOVO NORDISK A/S

FEI: 3003131673
Status: Active
Establishment types: Repack or Relabel Medical Device; Develop Specifications But Do Not Manufacture At This Facility
Owner/operator: NOVO NORDISK INC. (#9027307)

Address: BRENNUM PARK, HILLEROED Hovedstaden, DK-3400, DK

Mandatory US Agent: NOVO NORDISK INC.

## Products

Total registered: 1
Top product codes: KZH
Regulation §: 880.6920

Proprietary names: FLEXPRO PENMATE

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223003131673%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3003131673