SHEATHING TECHNOLOGIES, INC. 65-966-21815-3 Sheathes

K-WIRE Trocar POINT BOTH ENDS .035 x 4

Piston syringe without needle

The ENFit® Reusable Enteral Syringe is indicated for use as a dispenser, a measuring device and a fluid transfer device. It is used to deliver fluids into the body orally or enterally. It is intended to be used multiple times in non-clinical settings by users ranging from clinicians to laypersons in all age groups. The device is indicated for single patient use only.

First Aid Kit Wihout Drug (Content : Adhesive bandages in a variety of different sizes and shapes + Non-adherent sterile Gauze Pad + Cleansing wipe (with alcohol)) This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.

Looking to sell brand new Endoscope Guide devices by Olympus. They were purchased in 04/2018 for $17,900 and never opened. ScopeGuide UPD-3 is an exclusive Olympus technology designed to provide a real-time 3D image of the shape and position of the endoscope inside the body.

2108 Series Sagittal Blade (28.9 x 0.64 x 58.7mm)

Precision Thin Offset (10.0 x 0.38 x 43.0mm)

X-Ray Detectable Sponge, Sterile, 4" x 4", 16-Ply, 10 per tray

K-WIRE TROCAR POINT BOTH ENDS .062 X 4

Precision Reciprocating (22.5 x 0.64mm)

K-WIRE Trocar POINT BOTH ENDS .035 x 4

Piston syringe without needle

The ENFit® Reusable Enteral Syringe is indicated for use as a dispenser, a measuring device and a fluid transfer device. It is used to deliver fluids into the body orally or enterally. It is intended to be used multiple times in non-clinical settings by users ranging from clinicians to laypersons in all age groups. The device is indicated for single patient use only.

First Aid Kit Wihout Drug (Content : Adhesive bandages in a variety of different sizes and shapes + Non-adherent sterile Gauze Pad + Cleansing wipe (with alcohol)) This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.