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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, 12x22x50mm 10°
Nuvasive, Inc.
8221250P2
In Commercial Distribution

  • 00887517983305 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 10x22x55mm 10°
Nuvasive, Inc.
8221055P2
In Commercial Distribution

  • 00887517983244 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 10x22x50mm 10°
Nuvasive, Inc.
8221050P2
In Commercial Distribution

  • 00887517983220 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 8x22x55mm 10°
Nuvasive, Inc.
8220855P2
In Commercial Distribution

  • 00887517983169 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 12x18x55mm 10°
Nuvasive, Inc.
8181255P2
In Commercial Distribution

  • 00887517982841 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 12x18x50mm 10°
Nuvasive, Inc.
8181250P2
In Commercial Distribution

  • 00887517982827 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 10x18x55mm 10°
Nuvasive, Inc.
8181055P2
In Commercial Distribution

  • 00887517982766 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 10x18x50mm 10°
Nuvasive, Inc.
8181050P2
In Commercial Distribution

  • 00887517982742 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 8x18x55mm 10°
Nuvasive, Inc.
8180855P2
In Commercial Distribution

  • 00887517982681 ()


  • Polymeric spinal interbody fusion cage
COHERE XL, 8x18x50mm 10°
Nuvasive, Inc.
8180850P2
In Commercial Distribution

  • 00887517982667 ()


  • Polymeric spinal interbody fusion cage
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