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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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Analog Crystaline ST Liquid Crystal Temperature Trend Indicator
LCR HALLCREST, LLC.
6102H
In Commercial Distribution

  • 20815236020289 ()
  • 10815236020282 ()
  • 00815236020285 ()
6102H

  • Liquid-crystal patient thermometer, single-use
Analog Crystaline ST Liquid Crystal Temperature Trend Indicator
LCR HALLCREST, LLC.
6102F
In Commercial Distribution

  • 20815236020272 ()
  • 10815236020275 ()
  • 00815236020278 ()
6102F

  • Liquid-crystal patient thermometer, single-use
Analog Crystaline ST Liquid Crystal Temperature Trend Indicator
LCR HALLCREST, LLC.
6102C
In Commercial Distribution

  • 20815236020265 ()
  • 10815236020268 ()
  • 00815236020261 ()
6102C

  • Liquid-crystal patient thermometer, single-use
Analog Crystaline ST Liquid Crystal Temperature Trend Indicator
LCR HALLCREST, LLC.
6102B
In Commercial Distribution

  • 10815236020251 ()
  • 00815236020254 ()
6102B

  • Liquid-crystal patient thermometer, single-use
Analog Crystaline ST Liquid Crystal Temperature Trend Indicator
LCR HALLCREST, LLC.
6102
In Commercial Distribution

  • 30815236020248 ()
  • 20815236020241 ()
  • 10815236020244 ()
6102

  • Liquid-crystal patient thermometer, single-use
CUSTOM ADAPTER-BARD/ST.JUDE 10 LD
GRAPHIC CONTROLS ACQUISITION CORP
St Jude Medical
In Commercial Distribution

  • 03700506307104 ()
IPC73745

  • Patient monitoring system module, electrocardiographic
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
St. Jude Medical Probe Covers Clear Polyethylene Non-Sterile 9in x 96in x 1in 100 per Case
TIDI PRODUCTS, LLC
33431
Not in Commercial Distribution

  • 01618125183882 ()


  • Medical equipment/instrument drape, single-use
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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