BARD® LIFESTENT® Vascular and Biliary Stent System 6 mm x 20 mm (80 cm delivery catheter)

BARD® LIFESTENT® Vascular and Biliary Stent System 6 mm x 20 mm (130 cm delivery catheter)

BARD® LIFESTENT® Vascular and Biliary Stent System 6 mm x 30 mm (80 cm delivery catheter)

BARD® LIFESTENT® Vascular and Biliary Stent System 6 mm x 30 mm (130 cm delivery catheter)

BARD® LIFESTENT® Vascular and Biliary Stent System 6 mm x 40 mm (80 cm delivery catheter)

BARD® LIFESTENT® Vascular and Biliary Stent System 6 mm x 40 mm (130 cm delivery catheter)

BARD® LIFESTENT® Vascular and Biliary Stent System 6 mm x 60 mm (80 cm delivery catheter)

BARD® LIFESTENT® Vascular and Biliary Stent System 6 mm x 60 mm (130 cm delivery catheter)

BARD® LIFESTENT® Vascular and Biliary Stent System 6 mm x 80 mm (80 cm delivery catheter)

BARD® LIFESTENT® Vascular and Biliary Stent System 6 mm x 80 mm (130 cm delivery catheter)

BARD® LIFESTENT® XL Vascular and Biliary Stent System 6 mm x 100 mm (80 cm delivery catheter)

BARD® LIFESTENT® XL Vascular and Biliary Stent System 6 mm x 100 mm (130 cm delivery catheter)

BARD® LIFESTENT® XL Vascular and Biliary Stent System 6 mm x 120 mm (80 cm delivery catheter)

BARD® LIFESTENT® XL Vascular and Biliary Stent System 6 mm x 120 mm (130 cm delivery catheter)

BARD® LIFESTENT® XL Vascular and Biliary Stent System 6 mm x 150 mm (80 cm delivery catheter)

BARD® LIFESTENT® XL Vascular and Biliary Stent System 6 mm x 150 mm (130 cm delivery catheter)

BARD® LIFESTENT® XL Vascular Stent System 6 mm x 170 mm (80 cm delivery catheter)

BARD® LIFESTENT® XL Vascular Stent System 6 mm x 170 mm (130 cm delivery catheter)

BARD® LIFESTENT® Vascular and Biliary Stent System 7 mm x 20 mm (80 cm delivery catheter)

BARD® LIFESTENT® Vascular and Biliary Stent System 7 mm x 20 mm (130 cm delivery catheter)

BARD® LIFESTENT® Vascular and Biliary Stent System 7 mm x 30 mm (80 cm delivery catheter)

BARD® LIFESTENT® Vascular and Biliary Stent System 7 mm x 30 mm (130 cm delivery catheter)

BARD® LIFESTENT® Vascular and Biliary Stent System 7 mm x 40 mm (80 cm delivery catheter)

BARD® LIFESTENT® Vascular and Biliary Stent System 7 mm x 40 mm (130 cm delivery catheter)

BARD® LIFESTENT® Vascular and Biliary Stent System 7 mm x 60 mm (80 cm delivery catheter)

BARD® LIFESTENT® Vascular and Biliary Stent System 7 mm x 60 mm (130 cm delivery catheter)

BARD® LIFESTENT® Vascular and Biliary Stent System 7 mm x 80 mm (80 cm delivery catheter)

BARD® LIFESTENT® Vascular and Biliary Stent System 7 mm x 80 mm (130 cm delivery catheter)

BARD® LIFESTENT® XL Vascular and Biliary Stent System 7 mm x 100 mm (80 cm delivery catheter)

BARD® LIFESTENT® XL Vascular and Biliary Stent System 7 mm x 100 mm (130 cm delivery catheter)

BARD® LIFESTENT® XL Vascular and Biliary Stent System 7 mm x 120 mm (80 cm delivery catheter)

BARD® LIFESTENT® XL Vascular and Biliary Stent System 7 mm x 120 mm (130 cm delivery catheter)

BARD® LIFESTENT® XL Vascular and Biliary Stent System 7 mm x 150 mm (80 cm delivery catheter)

BARD® LIFESTENT® XL Vascular and Biliary Stent System 7 mm x 150 mm (130 cm delivery catheter)

BARD® LIFESTENT® XL Vascular Stent System 7 mm x 170 mm (80 cm delivery catheter)

BARD® LIFESTENT® XL Vascular Stent System 7 mm x 170 mm (130 cm delivery catheter)

Single use patient interface for the VisuMax laser keratome

The MEL 80 Excimer Laser System is indicated for use in primary Laser Assisted in situ Keratomileusis (LASIK) treatments for the reduction or elimination of - myopia of less than or equal to -7.0 D with or without refractive astigmatism of less than or equal to -3.0 D, with a Maximum MRSE of -7.0 D- naturally occurring hyperopia of less than or equal to +5.0 D with or without refractive astigmatism of greater than +0.5 D and less than or equal to +3.0 D, with a maximum MRSE of +5.0 D in patients who are 21 years of age or older with documentation of stable manifest refraction over the past year as demonstrated by Change in sphere and cylinder of 0.5 D.

The VisuMax laser keratome is a femtosecond laser. It generates a beam of ultra-short laser pulses whichare guided through the aperture in the treatment objective .The optical system focuses the laser beam into the corneal tissue.The VisuMax femtosecond laser is indicated for use in ophthalmic surgery for the creation of corneal incisions in patients undergoing the following treatments:• In the creation of a corneal flap in patients undergoing LASIK surgery or other treatment requiring initial lamellar resection of the cornea• In patients undergoing surgery or other treatment requiring initial lamellar resection of the cornea• In the creation of a lamellar cut/resection of the cornea for lamellar keratoplasty• In the creation of a cut/incision for penetrating keratoplasty and corneal harvesting• Surgery or other treatment requiring initial lamellar resection of the cornea to create tunnels for placement of corneal ring segments.Additionally under class III: The VisuMax Femtosecond Laser is indicated for use in small incisionlenticule extraction (SMILE) for the reduction or elimination ofmyopia with or without astigmatism• for spherical refractive error (in minus cylinder format) from -1.00 diopters through -10.00 diopters,• for cylinder from -0.75 diopters through -3.00 diopters,• when refraction spherical equivalent is no greater in magnitude than 10.00 diopters,in patients 22 years of age or older with documentation of stable manifest refraction over the past year as demonstrated by a change in sphere and cylinder of ≤ 0.50 D in magnitude.

The CustomFlex Artificial Iris is a prosthetic iris (the colored part of the eye around the pupil) made of thin, foldable medical-grade silicone. This device is custom-made and can be sized and colored for each individual patient. This with Fiber model has a polyester meshwork layer embedded in it to provide adequate tear strength to withstand suturing. The CustomFlex Artificial Iris can be used to treat congenital (genetic disorder in which the iris is completely or partially absent) and traumatic aniridia.It can also be used to treat iris defects due to other reasons or conditions, such as albinism, or surgical removal due to melanoma.

The CustomFlex Artificial Iris is a prosthetic iris (the colored part of the eye around the pupil) made of thin, foldable medical-grade silicone. This device is custom-made and can be sized and colored for each individual patient. This Fiber Free model is suitable for sutureless implant techniques or can be sutured.The CustomFlex Artificial Iris can be used to treat congenital (genetic disorder in which the iris is completely or partially absent) and traumatic aniridia.It can also be used to treat iris defects due to other reasons or conditions, such as albinism, or surgical removal due to melanoma.

The RIDASCREEN® Norovirus 3rd Generation EIA test is a qualitative enzyme immunoassay (EIA) intended for the detection of selected genogroup I (GI.1, GI.2, GI.3, GI.4, GI.7) and genogroup II (GII.1, GII.2, GII.3, GII.4, GII.5, GII.6, GII.7, GII.8, GII.10, GII.12, GII.13, GII.14, GII.17) norovirus strains in human feces as an aid in investigating the cause of acute gastroenteritis outbreaks.

The RIDASCREEN® Entamoeba histolytica IgG test is an enzyme immunoassay for the qualitative determination of IgG antibodies against Entamoeba histolytica in human serum. The test should be used for confirmation purposes when there is a suspected case of amoebiasis.

The RIDASCREEN® Echinococcus IgG test is an enzyme immunoassay for the qualitative determination of IgG antibodies against Echinococcus granulosus und Echinococcus multilocularis in human serum. The test should be used for confirmation purposes when there is a suspected case of infection with Echinococcus.

The RIDASCREEN® Taenia solium IgG test is an enzyme immunoassay for the qualitative determination of IgG antibodies against Taenia solium and its cysticerci (bladder worms) in human serum. The test should be used for confirmation purposes when there is a suspected case of infection with Taenia solium.

The RIDA®GENE Norovirus GI/GII assay, performed on the Applied Biosystems® 7500 Fast Dx System, is a real-time RT-PCR in vitro diagnostic test for the qualitative detection and differentiation of norovirus genogroup I (GI) and II (GII) RNA from raw or unpreserved stool specimens collected from individuals with signs and symptoms of acute gastroenteritis.