# AirLife Finland Oy

FEI: 3010838917
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Develop Specifications But Do Not Manufacture At This Facility
Owner/operator: SunMed Group Holdings, LLC dba AirLife (#10044795)

Address: Kuortaneenkatu 2, Helsinki Uusimaa, FIN-00510, FI

Mandatory US Agent: AirLife

## Products

Total registered: 2
Top product codes: DQA, DSA
Regulation §: 870.2700, 870.2900

Proprietary names: CABLE, TRANSDUCER AND ELECTRODE, PATIENT, Oximeter

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223010838917%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3010838917