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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.H10.3213
In Commercial Distribution

  • 08800017217505 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.3212
In Commercial Distribution

  • 08800017217499 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.3211
In Commercial Distribution

  • 08800017217482 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.3210
In Commercial Distribution

  • 08800017217475 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.3209
In Commercial Distribution

  • 08800017217468 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.3208
In Commercial Distribution

  • 08800017217451 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.2916
In Commercial Distribution

  • 08800017217444 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.2915
In Commercial Distribution

  • 08800017217437 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.2914
In Commercial Distribution

  • 08800017217420 ()


  • Polymeric spinal interbody fusion cage
LOSPA IS TLIF Cage B Type (Non-sterile)
Corentec Co., Ltd
SC.H10.2913
In Commercial Distribution

  • 08800017217413 ()


  • Polymeric spinal interbody fusion cage
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