RODO MEDICAL, INC. 50010STB221 Smileloc® BY RODO

Band-Lok® is a two paste dual-cure adhesive intended for use as a band cement.Band-Lok Product Features:No messy Powder-Liquid Systems. Consistent mix viscosity every timeUnlike Glass Monomer cements, Band-Lok does not have an aftertaste or odor.Better adhesion to enamel and band surfaces is achieved, reducing washout and preventing loose bandsFour minute working time at room temperature without a frozen slab.Band-Lok is a Dual Cure cement. It can be used with or without a dental curing light. When band is placed and flash is cleaned a 20 second light activation allows full protection from moisture. Without light activation a complete set is achieved in 10 minutes.Superior Adhesion/Reduced Washout: Band-Lok is a unique combination of Resin and Glass Ionomer technology.Band-Lok is Fluoride releasing.Contents of Kit:•(4) 6gm. Syringes of Part A Paste•(4) 6gm. Syringes of Part B Paste•Mixing Pads and Spatulas.

Recline (2-point) Adjustable Height Armrest Assembly attaches to the recline back cane and seat side frame. The Recline Armrest is designed to flip backward to provide clearance for side transfers. Two height ranges available (9"-13" or 13"-16"). Left and Right armrest configurations available. Optional wheelchair component for use with Motion Concepts power positioning systems

The Rconsole1 is intended for use with mammographic images acquired using digital breast x-ray systems.

NB-BVP-F (finger module):The BVP sensor provides a photoplethysmography (PPG) signal when connected to a NeXus signal acquisition device, that corresponds with variations in peripheral blood flow resulting from cardiovascular activity and responses, with the purpose of providing information on the cardiovascular variations such as heart rate variations and measured pulse amplitude. The sensor output is not intended to be used for vital monitoring purposes.The device is designed for medical use, not restricted to a specific medical indication, for acquisition of physiological signals. The device is intended to be used by, or under supervision of, a health professional within a clinical environment.