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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 XLW, 8x22x60mm 10°
Nuvasive, Inc.
8220860P2
In Commercial Distribution

  • 00887517983183 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 8x22x45mm 10°
Nuvasive, Inc.
8220845P2
In Commercial Distribution

  • 00887517983121 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 8x18x60mm 0°
Nuvasive, Inc.
8187860P2
In Commercial Distribution

  • 00887517983107 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 8x18x55mm 0°
Nuvasive, Inc.
8187855P2
In Commercial Distribution

  • 00887517983084 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 8x18x50mm 0°
Nuvasive, Inc.
8187850P2
In Commercial Distribution

  • 00887517983060 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 8x18x45mm 0°
Nuvasive, Inc.
8187845P2
In Commercial Distribution

  • 00887517983046 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 12x18x60mm 0°
Nuvasive, Inc.
8187260P2
In Commercial Distribution

  • 00887517983022 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 12x18x55mm 0°
Nuvasive, Inc.
8187255P2
In Commercial Distribution

  • 00887517983008 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 12x18x50mm 0°
Nuvasive, Inc.
8187250P2
In Commercial Distribution

  • 00887517982988 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 12x18x45mm 0°
Nuvasive, Inc.
8187245P2
In Commercial Distribution

  • 00887517982964 ()


  • Polymeric spinal interbody fusion cage
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