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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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TLIF HOLDER STRAIGHT, OUS TYPE
Corentec Co., Ltd
SI.C30.0003
In Commercial Distribution

  • 08800017273914 ()


  • Surgical implant/trial-implant/sizer holder, reusable
TLIF HOLDER CURVED
Corentec Co., Ltd
SI.C30.0002
In Commercial Distribution

  • 08800017273907 ()


  • Surgical implant/trial-implant/sizer holder, reusable
TLIF HOLDER STRAIGHT
Corentec Co., Ltd
SI.C30.0001
In Commercial Distribution

  • 08800017273891 ()


  • Surgical implant/trial-implant/sizer holder, reusable
Pedicle screw(Guided, Blasting)
Corentec Co., Ltd
01.27.616
In Commercial Distribution

  • 08800017226552 ()


  • Bone-screw internal spinal fixation system, non-sterile
LOSPA IS DLIF Cage (Non-sterile)
Corentec Co., Ltd
SC.V08.6016
In Commercial Distribution

  • 08800017222936 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS DLIF Cage (Non-sterile)
Corentec Co., Ltd
SC.V08.6014
In Commercial Distribution

  • 08800017222929 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS DLIF Cage (Non-sterile)
Corentec Co., Ltd
SC.V08.6012
In Commercial Distribution

  • 08800017222912 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS DLIF Cage (Non-sterile)
Corentec Co., Ltd
SC.V08.5516
In Commercial Distribution

  • 08800017222905 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS DLIF Cage (Non-sterile)
Corentec Co., Ltd
SC.V08.5514
In Commercial Distribution

  • 08800017222899 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS DLIF Cage (Non-sterile)
Corentec Co., Ltd
SC.V08.5512
In Commercial Distribution

  • 08800017222882 ()


  • Polymeric spinal interbody fusion cage
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