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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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Bidirectional Steerable Diagnostic Catheter
BOSTON SCIENTIFIC CORPORATION
M0043200080
Not in Commercial Distribution

  • 08714729877837 ()

  • 2.33 mm Diameter
  • 7 F Diameter


  • Cardiac mapping catheter, percutaneous, single-use
Bidirectional Steerable Diagnostic Catheter
BOSTON SCIENTIFIC CORPORATION
M0043200070
Not in Commercial Distribution

  • 08714729877820 ()

  • 2.33 mm Diameter
  • 7 F Diameter


  • Cardiac mapping catheter, percutaneous, single-use
Bidirectional Steerable Diagnostic Catheter
BOSTON SCIENTIFIC CORPORATION
M0043200060
Not in Commercial Distribution

  • 08714729877813 ()

  • 2.33 mm Diameter
  • 7 F Diameter


  • Cardiac mapping catheter, percutaneous, single-use
Bidirectional Steerable Diagnostic Catheter
BOSTON SCIENTIFIC CORPORATION
M0043200050
Not in Commercial Distribution

  • 08714729877806 ()

  • 7 F Diameter
  • 2.33 mm Diameter


  • Cardiac mapping catheter, percutaneous, single-use
Bidirectional Steerable Diagnostic Catheter
BOSTON SCIENTIFIC CORPORATION
M0043200030
Not in Commercial Distribution

  • 08714729877783 ()

  • 2.33 mm Diameter
  • 7 F Diameter


  • Cardiac mapping catheter, percutaneous, single-use
Bidirectional Steerable Diagnostic Catheter
BOSTON SCIENTIFIC CORPORATION
M0043200020
Not in Commercial Distribution

  • 08714729877776 ()

  • 2.33 mm Diameter
  • 7 F Diameter


  • Cardiac mapping catheter, percutaneous, single-use
Bidirectional Steerable Diagnostic Catheter
BOSTON SCIENTIFIC CORPORATION
M0043200010
Not in Commercial Distribution

  • 08714729877769 ()

  • 2.33 mm Diameter
  • 7 F Diameter


  • Cardiac mapping catheter, percutaneous, 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
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

  • 04047844114230 ()

  • 15x10x32mm
TST20151032

  • Metallic spinal interbody fusion cage
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