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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-W+, 9x22x50mm
Nuvasive, Inc.
6509250P2
In Commercial Distribution

  • 00887517993533 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-W+, 9x22x45mm
Nuvasive, Inc.
6509245P2
In Commercial Distribution

  • 00887517993526 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-W+, 7x22x60mm
Nuvasive, Inc.
6507260P2
In Commercial Distribution

  • 00887517993519 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-W+, 7x22x55mm
Nuvasive, Inc.
6507255P2
In Commercial Distribution

  • 00887517993502 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-W+, 7x22x50mm
Nuvasive, Inc.
6507250P2
In Commercial Distribution

  • 00887517993496 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-W+, 7x22x45mm
Nuvasive, Inc.
6507245P2
In Commercial Distribution

  • 00887517993489 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-W+, 6x22x60mm
Nuvasive, Inc.
6506260P2
In Commercial Distribution

  • 00887517993472 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-W+, 6x22x55mm
Nuvasive, Inc.
6506255P2
In Commercial Distribution

  • 00887517993465 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-W+, 6x22x50mm
Nuvasive, Inc.
6506250P2
In Commercial Distribution

  • 00887517993458 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL-W+, 6x22x45mm
Nuvasive, Inc.
6506245P2
In Commercial Distribution

  • 00887517993441 ()


  • Polymeric spinal interbody fusion cage
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