# DPM USA CORP.

FEI: 3001779742
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: DPM USA CORP. (#9008401)

Address: 1460 N.W. 107TH AVE., STE. G, Doral, FL, US



## Products

Total registered: 1
Top product codes: EFA
Regulation §: 872.4200

Proprietary names: Tubinetta Fit Lux, Tubinetta Ultra, Switch E, Bogotta Light Plus, Bogota Stilla Prime

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223001779742%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3001779742