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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 TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H17.2411
In Commercial Distribution

  • 08800017217659 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H17.2410
In Commercial Distribution

  • 08800017217642 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H17.2409
In Commercial Distribution

  • 08800017217635 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.3516
In Commercial Distribution

  • 08800017217628 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.3515
In Commercial Distribution

  • 08800017217611 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.3514
In Commercial Distribution

  • 08800017217604 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.3513
In Commercial Distribution

  • 08800017217598 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.3512
In Commercial Distribution

  • 08800017217581 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.3511
In Commercial Distribution

  • 08800017217574 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.3510
In Commercial Distribution

  • 08800017217567 ()


  • Polymeric spinal interbody fusion cage
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