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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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Modulus TLIF-O, 8x10x30mm 4°
Nuvasive, Inc.
2080304P2
In Commercial Distribution

  • 00887517879059 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 8x10x30mm 12°
Nuvasive, Inc.
2080302P2
In Commercial Distribution

  • 00887517879035 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 8x10x25mm 8°
Nuvasive, Inc.
2080258P2
In Commercial Distribution

  • 00887517878991 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 8x10x25mm 4°
Nuvasive, Inc.
2080254P2
In Commercial Distribution

  • 00887517878953 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 8x10x25mm 12°
Nuvasive, Inc.
2080252P2
In Commercial Distribution

  • 00887517878939 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 7x10x30mm 8°
Nuvasive, Inc.
2070308P2
In Commercial Distribution

  • 00887517878298 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 7x10x30mm 4°
Nuvasive, Inc.
2070304P2
In Commercial Distribution

  • 00887517878250 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 7x10x30mm 12°
Nuvasive, Inc.
2070302P2
In Commercial Distribution

  • 00887517878236 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 7x10x25mm 8°
Nuvasive, Inc.
2070258P2
In Commercial Distribution

  • 00887517878199 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 7x10x25mm 4°
Nuvasive, Inc.
2070254P2
In Commercial Distribution

  • 00887517878151 ()


  • Metallic spinal interbody fusion cage
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