# CELLAVISION AB

FEI: 3003630693
Status: Active
Establishment types: Develop Specifications But Do Not Manufacture At This Facility; Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device; Export Device to the United States But Perform No Other Operation on Device
Owner/operator: CellaVision AB (#9043433)

Address: Mobilvagen 12, LUND Skane, SE-22362, SE

Mandatory US Agent: -

## Products

Total registered: 2
Top product codes: GKZ, JOY
Regulation §: 864.5220, 864.5260

Proprietary names: CellaVision DM96

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223003630693%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3003630693