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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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SEBIA
2057
In Commercial Distribution

  • 03607360020579 ()
2057

  • Carbohydrate deficient transferrin IVD, reagent
Set screw Wrong DI Number
Corentec Co., Ltd
00.00.0000
In Commercial Distribution

  • 08806373812910 ()


  • Bone-screw internal spinal fixation system, non-sterile
Pedicle screw(Standard, Blasting+Anodizing)
Corentec Co., Ltd
01.22.607
In Commercial Distribution

  • 08806373811388 ()


  • Bone-screw internal spinal fixation system, non-sterile
Sleeve
Corentec Co., Ltd
01.21.010
In Commercial Distribution

  • 08806373810459 ()


  • Bone-screw internal spinal fixation system, non-sterile
Rod-B
Corentec Co., Ltd
01.21.073
In Commercial Distribution

  • 08806373837005 ()


  • Bone-screw internal spinal fixation system, non-sterile
Pedicle screw
Corentec Co., Ltd
01.21.558
In Commercial Distribution

  • 08806373810855 ()


  • Bone-screw internal spinal fixation system, non-sterile
Pedicle screw(Guided, Blasting) DI should be "08800017226552"
Corentec Co., Ltd
01.27.616
In Commercial Distribution

  • 08806373816130 ()


  • Bone-screw internal spinal fixation system, non-sterile
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 (Sterile)
Corentec Co., Ltd
SC.V58.6016
In Commercial Distribution

  • 08800017224596 ()


  • Polymeric spinal fusion cage, sterile
LOSPA IS DLIF Cage (Sterile)
Corentec Co., Ltd
SC.V58.6014
In Commercial Distribution

  • 08800017224589 ()


  • Polymeric spinal fusion cage, sterile
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