# EVO DI BRIDDA MASSIMO

FEI: 3010862420
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer); Complaint File Establishment per 21 CFR 820.198; Sterilize Medical Device for Another Party (Contract Sterilizer); Remanufacture Medical Device; Repack or Relabel Medical Device; Foreign Private Label Distributor; Export Device to the United States But Perform No Other Operation on Device; Develop Specifications But Do Not Manufacture At This Facility; Reprocess Single-Use Device; Manufacture Medical Device
Owner/operator: EVO DI BRIDDA MASSIMO (#10046465)

Address: VIA FELTRE 52/M, SEDICO Belluno, 32036, IT

Mandatory US Agent: THE VISION COUNCIL

## Products

Total registered: 1
Top product codes: HQY
Regulation §: 886.5850


## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223010862420%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3010862420