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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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CoRoent XL+, 15x18x40mm 15°
Nuvasive, Inc.
7161540
In Commercial Distribution

  • 00887517731586 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 14x18x65mm 15°
Nuvasive, Inc.
7161465
In Commercial Distribution

  • 00887517731562 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 14x18x60mm 15°
Nuvasive, Inc.
7161460
In Commercial Distribution

  • 00887517731548 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 14x18x55mm 15°
Nuvasive, Inc.
7161455
In Commercial Distribution

  • 00887517731524 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 14x18x50mm 15°
Nuvasive, Inc.
7161450
In Commercial Distribution

  • 00887517731500 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 14x18x45mm 15°
Nuvasive, Inc.
7161445
In Commercial Distribution

  • 00887517731487 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 14x18x40mm 15°
Nuvasive, Inc.
7161440
In Commercial Distribution

  • 00887517731463 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 13x18x65mm 15°
Nuvasive, Inc.
7161365
In Commercial Distribution

  • 00887517731449 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 13x18x60mm 15°
Nuvasive, Inc.
7161360
In Commercial Distribution

  • 00887517731425 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL+, 13x18x55mm 15°
Nuvasive, Inc.
7161355
In Commercial Distribution

  • 00887517731401 ()


  • Polymeric spinal interbody fusion cage
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