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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.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
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.3509
In Commercial Distribution

  • 08800017217550 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.3508
In Commercial Distribution

  • 08800017217543 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.3216
In Commercial Distribution

  • 08800017217536 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.3215
In Commercial Distribution

  • 08800017217529 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.3214
In Commercial Distribution

  • 08800017217512 ()


  • Polymeric spinal interbody fusion cage
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