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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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RUAS/SS ST 559200023 ST 4.75/5.0 RUAS/SS
MEDTRONIC SOFAMOR DANEK, INC.
559200023
In Commercial Distribution

  • 00763000972714 ()


  • Spinal bone screw, non-bioabsorbable
RMAS/SS ST 559200021 ST 4.75/5.0 RMAS/SS
MEDTRONIC SOFAMOR DANEK, INC.
559200021
In Commercial Distribution

  • 00763000972691 ()


  • Spinal bone screw, non-bioabsorbable
Dental anaesthesia injection kit
FAIRFAX MEDICAL PRODUCTS LIMITED
Stabident Standard kit
In Commercial Distribution

  • 05060489370167 ()
  • 05060489370136 ()
ST

  • Dental anaesthesia injection kit
St. Jude Medical Probe Covers Clear Polyethylene Sterile 9in x 96in x 1in 100 per Case
TIDI PRODUCTS, LLC
30965
Not in Commercial Distribution

  • 00618125167883 ()
  • 01618125167882 ()


  • Medical equipment/instrument drape, single-use
Short Tip Microwave Antenna Kit (20 cm, 1 per Tray)
VARIAN MEDICAL SYSTEMS, INC.
22-17025-320
In Commercial Distribution

  • 00810563021042 ()
SWST-1420

  • Microwave ablation system probe, non-powered
Short Tip Microwave Antenna Kit (15 cm, 1 per Tray)
VARIAN MEDICAL SYSTEMS, INC.
22-17025-315
In Commercial Distribution

  • 00810563021035 ()
SWST-1415

  • Microwave ablation system probe, non-powered
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
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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