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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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No Description
implantcast GmbH
02803439
In Commercial Distribution

  • 04048844355692 ()

  • Size 32/39mm


  • Non-constrained polyethylene acetabular liner
No Description
BIOPRO, INC.
19132
In Commercial Distribution

  • M209191320 ()


  • Metal-on-polyethylene total hip prosthesis
No Description
BIOPRO, INC.
18594
In Commercial Distribution

  • M209185940 ()


  • Metal-on-polyethylene total hip prosthesis
No Description
BIOPRO, INC.
18589
In Commercial Distribution

  • M209185890 ()


  • Metal-on-polyethylene total hip prosthesis
No Description
BIOPRO, INC.
19054
In Commercial Distribution

  • M209190540 ()


  • Metal-on-polyethylene total hip prosthesis
No Description
BIOPRO, INC.
19005
In Commercial Distribution

  • M209190050 ()


  • Metal-on-polyethylene total hip prosthesis
No Description
Trilliant Surgical, LLC
300-85-014
In Commercial Distribution

  • 00810028395664 ()


  • Orthopaedic fixation plate, non-bioabsorbable
No Description
Trilliant Surgical, LLC
300-85-011
In Commercial Distribution

  • 00810028395633 ()


  • Orthopaedic fixation plate, non-bioabsorbable
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, straight
In Commercial Distribution

  • 04047844115923 ()

  • 16x9x32mm
TRT00160932

  • 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, straight
In Commercial Distribution

  • 04047844115916 ()

  • 15x9x32mm
TRT00150932

  • Metallic spinal interbody fusion cage
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