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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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CONSTRUX PILLAR IMPL CASE TL EZ IN
Orthofix US LLC
45-0094
In Commercial Distribution

  • 18257200036837 ()


  • Metallic spinal interbody fusion cage
CONSTRUX PILLAR IMPL CASE PL EZ IN
Orthofix US LLC
45-0093
In Commercial Distribution

  • 18257200036820 ()


  • Metallic spinal interbody fusion cage
Lumbar Interbody Fusion System (OLLIF) Instrument Set in Sterilization Case
ADVANCED RESEARCH MEDICAL LLC
01-2001
In Commercial Distribution

  • 00850014575038 ()
01-2001

  • Instrument tray, reusable
  • Metallic spinal interbody fusion cage
Lumbar Interbody Fusion System (OLLIF) Oblique 33 mm Implants in Caddy
ADVANCED RESEARCH MEDICAL LLC
O-3300
In Commercial Distribution

  • 00850014575342 ()
O-3300

  • Instrument tray, reusable
  • Metallic spinal interbody fusion cage
Lumbar Interbody Fusion System (OLLIF) Oblique 30 mm Implants in Caddy
ADVANCED RESEARCH MEDICAL LLC
O-3000
In Commercial Distribution

  • 00850014575335 ()
O-3000

  • Instrument tray, reusable
  • Metallic spinal interbody fusion cage
Lumbar Interbody Fusion System (OLLIF) Oblique 27 mm Implants in Caddy
ADVANCED RESEARCH MEDICAL LLC
O-2700
In Commercial Distribution

  • 00850014575328 ()
O-2700

  • Instrument tray, reusable
  • Metallic spinal interbody fusion cage
Lumbar Interbody Fusion System (OLLIF) Instrument Set in Graphic Sterilization Case
ADVANCED RESEARCH MEDICAL LLC
01-2000
In Commercial Distribution

  • 00850014575021 ()
01-2000

  • Instrument tray, reusable
  • 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

  • 04047844116258 ()

  • 18x9x32mm
TRT20180932

  • 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

  • 04047844116241 ()

  • 17x9x32mm
TRT20170932

  • 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

  • 04047844116234 ()

  • 16x9x32mm
TRT20160932

  • Metallic spinal interbody fusion cage
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