# TD SYNNEX

FEI: 3026740087
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner/operator: TD SYNNEX (#10087381)

Address: 5300 Centerpoint Pkwy, Groveport, OH, US



## Products

Total registered: 1
Top product codes: CBK
Regulation §: 868.5895

Proprietary names: Trilogy 200

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223026740087%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3026740087