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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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LOSPA IS ACP RST 1 Level (Non-sterile)
Corentec Co., Ltd
SM.C01.0220
In Commercial Distribution

  • 08800017218649 ()


  • Spinal fixation plate, non-bioabsorbable
LOSPA IS ACP RST 1 Level (Non-sterile)
Corentec Co., Ltd
SM.C01.0200
In Commercial Distribution

  • 08800017218632 ()


  • Spinal fixation plate, non-bioabsorbable
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H17.3516
In Commercial Distribution

  • 08800017217949 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H17.3515
In Commercial Distribution

  • 08800017217932 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H17.3514
In Commercial Distribution

  • 08800017217925 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H17.3513
In Commercial Distribution

  • 08800017217918 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H17.3512
In Commercial Distribution

  • 08800017217901 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H17.3511
In Commercial Distribution

  • 08800017217895 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H17.3510
In Commercial Distribution

  • 08800017217888 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H17.3509
In Commercial Distribution

  • 08800017217871 ()


  • Polymeric spinal interbody fusion cage
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