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THE RUHOF CORPORATION

FEI 3003207991 · Repack or Relabel Medical Device Manufacture Medical Device · Status: Active

FEI Number3003207991
Owner / OperatorThe Ruhof Corporation (#10038187)
Address393 Sagamore Ave, Mineola, NY, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)MNL
Regulation § (21 CFR)876.1500
Proprietary namesTest 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

External sources

Source: openFDA. Public-domain (CC0).