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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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Linear ST, 50cm 8 Contact Lead Kit
BOSTON SCIENTIFIC NEUROMODULATION CORPORATION
SC-2218-50
In Commercial Distribution

  • M365SC2218500 ()

  • 50 cm Length
SC-2218-50

  • Analgesic spinal cord electrical stimulation system
Symmetry® Retractor, St. Marks Deep Pelvic, w/Lip, 15° Angle, 11 in Working Length
SYMMETRY SURGICAL INC.
50-9028S
In Commercial Distribution

  • 00887482074800 ()

  • Angle: 15 degree
  • Length: 11 Inch
50-9028S

  • Hand-held surgical retractor, reusable
Symmetry® Retractor, St Marks Deep Pelvic, 15° Angle, w/Lip, 9 in Working Length, 13 2/5 in, 34 cm
SYMMETRY SURGICAL INC.
50-9027S
In Commercial Distribution

  • 00887482074794 ()

  • Angle: 15 degree
  • Length: 13.4 Inch
50-9027S

  • Hand-held surgical retractor, reusable
Symmetry® Retractor, St. Marks Deep Pelvic, w/Lip, 15° Angle, 7 in Blade Length, 13 in, 330 mm
SYMMETRY SURGICAL INC.
50-9025S
In Commercial Distribution

  • 00887482074770 ()

  • Angle: 15 degree
  • Length: 13 Inch
50-9025S

  • Hand-held surgical retractor, reusable
Symmetry® Forceps, St. Clair, Adenoid, 5 mm x 10 mm Ring Jaw, 7 5/8 in
SYMMETRY SURGICAL INC.
71-5018
In Commercial Distribution

  • 00887482122495 ()

  • Width: 5 Millimeter
  • Depth: 10 Millimeter
  • Length: 7.625 Inch
71-5018

  • Dressing/utility forceps, scissors-like, reusable
Glaucoma shunt
NEW WORLD MEDICAL, INCORPORATED
ST350
In Commercial Distribution

  • 00892064002096 ()

  • Area/Surface Area: 350 Square millimeter
10-0610

  • Glaucoma shunt, tubular, non-animal-derived
Glaucoma shunt
NEW WORLD MEDICAL, INCORPORATED
ST250
In Commercial Distribution

  • 00892064002089 ()

  • Area/Surface Area: 250 Square millimeter
10-0609

  • Glaucoma shunt, tubular, non-animal-derived
70cm 8 Contact Trial Lead Kit
BOSTON SCIENTIFIC NEUROMODULATION CORPORATION
SC-2218-70E
In Commercial Distribution

  • 08714729820741 ()

  • 70 cm Length


  • Implantable electrical stimulation system intraoperative test lead
The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, angled
In Commercial Distribution

  • 04047844114254 ()

  • 17x10x32mm
TST20171032

  • Metallic spinal interbody fusion cage
The SIGNUS TETRIS™ ST and SIGNUS TETRIS™ R ST system is an intervertebral fusion device to treat degenerative disc disease. The implants are additively manufactured from titanium alloy (Ti-6Al-4V). Each device is available in a single footprint, with multiple heights and angulations. The SIGNUS TETRIS™ ST/ TETRIS™ R ST device is placed by a PLIF (Posterior Lumbar Interbody Fusion) approach in the L2 – S1 spinal region and should be inserted in pairs. The device is comprised of structural titanium in an open-pore grid structure. The large fenestration in the implant permits the cage to be packed with autogenous bone graft and/or allograft comprised of cancellous and/or corticocancellous bone graft to facilitate fusion.
SIGNUS Medizintechnik GmbH
Lumbar cage, angled
In Commercial Distribution

  • 04047844114247 ()

  • 16x10x32mm
TST20161032

  • Metallic spinal interbody fusion cage
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