# V. GULDMANN A/S

FEI: 3002835648
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: V. GULDMANN A/S (#9027662)

Address: GRAHAM BELLS VEJ 23 A, AARHUS N Midtjylland, DK-8200, DK

Mandatory US Agent: Guldmann Inc.

## Products

Total registered: 1
Top product codes: FSA
Regulation §: 880.5510

Proprietary names: GH3  Twin Patient Lift, GH1 F  Patient Lift, GH1  Patient Lift, GL5.2  Patient Floor Lift, GH3  Patient Lift, GH1 Q  Patient Lift, GHZ  Patient Lift, GLS5.2  Sit to Stand Floor Lifter, GH3+  Patient Lift

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223002835648%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3002835648