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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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COHERE XL, 10x18x55mm 15°
Nuvasive, Inc.
8105515P2
In Commercial Distribution

  • 00887517982049 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 10x18x50mm 15°
Nuvasive, Inc.
8105015P2
In Commercial Distribution

  • 00887517982025 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 10x18x45mm 15°
Nuvasive, Inc.
8104515P2
In Commercial Distribution

  • 00887517982001 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 8x18x60mm 15°
Nuvasive, Inc.
8086015P2
In Commercial Distribution

  • 00887517981981 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 8x18x55mm 15°
Nuvasive, Inc.
8085515P2
In Commercial Distribution

  • 00887517981967 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 8x18x50mm 15°
Nuvasive, Inc.
8085015P2
In Commercial Distribution

  • 00887517981943 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 8x18x45mm 15°
Nuvasive, Inc.
8084515P2
In Commercial Distribution

  • 00887517981929 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 9x22x60mm 10°
Nuvasive, Inc.
6309260
In Commercial Distribution

  • 00887517305855 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 9x22x55mm 10°
Nuvasive, Inc.
6309255
In Commercial Distribution

  • 00887517305848 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-W+, 9x22x50mm 10°
Nuvasive, Inc.
6309250
In Commercial Distribution

  • 00887517305831 ()


  • Polymeric spinal interbody fusion cage
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