# MELOQ AB

FEI: 3013687630
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: Meloq AB (#10056849)

Address: Brannkyrkagatan 72, Stockholm, 118 23, SE

Mandatory US Agent: J & D CAMPBELL ASSOCIATES, INC.

## Products

Total registered: 1
Top product codes: KQX
Regulation §: 888.1500


## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223013687630%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3013687630