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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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S-ROM ZTT - 10603295175636

S-ROM Total Hip System ZTT Oversize Proximal Sleeve POROUS COATED 24 F SML FITS: 22 x 17 STEM Cone: F Triangle: SML 22 INTERNAL DIAMETER
DEPUY ORTHOPAEDICS, INC.
55-0747
In Commercial Distribution

  • 10603295175636 ()
550747

  • Sleeve femoral/tibial extension, coated

S-ROM ZTT - 10603295175711

S-ROM Total Hip System ZTT Undersize Proximal Sleeve POROUS COATED 24 F XXL FITS: 26 x 21 STEM Cone: F Triangle: XXL 26 INTERNAL DIAMETER
DEPUY ORTHOPAEDICS, INC.
55-0779
In Commercial Distribution

  • 10603295175711 ()
550779

  • Sleeve femoral/tibial extension, coated

S-ROM ZTT - 10603295175698

S-ROM Total Hip System ZTT Undersize Proximal Sleeve POROUS COATED 24 F SML FITS: 26 x 21 STEM Cone: F Triangle: SML 26 INTERNAL DIAMETER
DEPUY ORTHOPAEDICS, INC.
55-0777
In Commercial Distribution

  • 10603295175698 ()
550777

  • Sleeve femoral/tibial extension, coated

S-ROM ZTT - 10603295175674

S-ROM Modular Hip System ZTT Undersize Proximal Sleeve POROUS COATED 24 D LRG FITS: 26 x 21 STEM Cone: D Triangle: LRG 26 INTERNAL DIAMETER
DEPUY ORTHOPAEDICS, INC.
55-0771
In Commercial Distribution

  • 10603295175674 ()
550771

  • Sleeve femoral/tibial extension, coated

S-ROM ZTT - 10603295175650

S-ROM Total Hip System ZTT Oversize Proximal Sleeve POROUS COATED 24 F XXL FITS: 22 x 17 STEM Cone: F Triangle: XXL 22 INTERNAL DIAMETER
DEPUY ORTHOPAEDICS, INC.
55-0751
In Commercial Distribution

  • 10603295175650 ()
550751

  • Sleeve femoral/tibial extension, coated

S-ROM ZTT - 10603295175643

S-ROM Total Hip System ZTT Oversize Proximal Sleeve POROUS COATED 24 F LRG FITS: 22 x 17 STEM Cone: F Triangle: LRG 22 INTERNAL DIAMETER
DEPUY ORTHOPAEDICS, INC.
55-0748
In Commercial Distribution

  • 10603295175643 ()
550748

  • Sleeve femoral/tibial extension, coated

MEL 80 - 04049471000221

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.
Carl Zeiss Meditec AG
MEL 80
In Commercial Distribution

  • 04049471000221 ()

  • Weight: 260 Kilogram
  • LxWxH: 1.55m x 0.80m x1.49m


  • Ophthalmic excimer laser system

TALENT® OCCLUDER - 00763000233792

STENT GRAFT OCL24US 24MM OCCLUDER
MEDTRONIC, INC.
OCL24US
Not in Commercial Distribution

  • 00763000233792 ()

  • Stent Graft Covered Length 35 MM
  • Stent Graft Diameter 24 MM


  • Abdominal aorta endovascular stent-graft

RelayPro Thoracic Stent-Graft System - 00843576164765

Endovascular Stent-Graft System
Bolton Medical Inc.
28-N4-24-230-24U
In Commercial Distribution

  • 00843576164765 ()

  • Outer Diameter: 24 Millimeter
  • Length: 229 Millimeter
  • Catheter Gauge: 19 French
28-N4-24-230-24U

  • Descending thoracic aorta endovascular stent-graft

RelayPro Thoracic Stent-Graft System - 00843576164758

Endovascular Stent-Graft System
Bolton Medical Inc.
28-N4-24-210-24U
In Commercial Distribution

  • 00843576164758 ()

  • Outer Diameter: 24 Millimeter
  • Length: 208 Millimeter
  • Catheter Gauge: 19 French
28-N4-24-210-24U

  • Descending thoracic aorta endovascular stent-graft
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