# BIOPORTO DIAGNOSTICS A/S

FEI: 3010739981
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: BioPorto Diagnostics A/S (#10089659)

Address: Tuborg Havnevej, 15, st, Hellerup Hovedstaden, 2900, DK



## Products

Total registered: 1
Top product codes: PIG
Regulation §: 862.1220

Proprietary names: ProNephro AKI™ (NGAL)

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223010739981%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3010739981