# THE RUHOF CORPORATION

FEI: 3003207991
Status: Active
Establishment types: Repack or Relabel Medical Device; Manufacture Medical Device
Owner/operator: The Ruhof Corporation (#10038187)

Address: 393 Sagamore Ave, Mineola, NY, US



## Products

Total registered: 1
Top product codes: MNL
Regulation §: 876.1500

Proprietary names: Test Instrusponge, ScopeValet Dual End 2 in 1 Channel/Valve Brush, Endozime Sponge, ScopeValet Endo Brush 345EBL, Endozime InstruSponge, ScopeValet Endo Brush 345EBS, 345CKENT Custom Kit, GVEBL, Safestep Test Instrusponge, G4VB

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223003207991%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3003207991