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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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BASE Ti HL Implant, 10x38x28mm 20°
Nuvasive, Inc.
6952020
In Commercial Distribution

  • 00887517700902 ()


  • Metallic spinal interbody fusion cage
BASE Ti HL Implant, 8x34x24mm 20°
Nuvasive, Inc.
6951820
In Commercial Distribution

  • 00887517700834 ()


  • Metallic spinal interbody fusion cage
BASE Ti HL Implant, 6x34x24mm 20°
Nuvasive, Inc.
6951620
In Commercial Distribution

  • 00887517700780 ()


  • Metallic spinal interbody fusion cage
BASE Ti HL Implant, 14x34x24mm 20°
Nuvasive, Inc.
6951420
In Commercial Distribution

  • 00887517700735 ()


  • Metallic spinal interbody fusion cage
BASE Ti HL Implant, 12x34x24mm 20°
Nuvasive, Inc.
6951220
In Commercial Distribution

  • 00887517700667 ()


  • Metallic spinal interbody fusion cage
BASE Ti HL Implant, 10x34x24mm 20°
Nuvasive, Inc.
6951020
In Commercial Distribution

  • 00887517700599 ()


  • Metallic spinal interbody fusion cage
BASE Ti HL Implant, 14x34x28mm 20°
Nuvasive, Inc.
6959014
In Commercial Distribution

  • 00887517702630 ()


  • Metallic spinal interbody fusion cage
BASE Ti HL Implant, 12x34x28mm 20°
Nuvasive, Inc.
6959013
In Commercial Distribution

  • 00887517702623 ()


  • Metallic spinal interbody fusion cage
BASE Ti HL Implant, 10x34x28mm 20°
Nuvasive, Inc.
6959012
In Commercial Distribution

  • 00887517702616 ()


  • Metallic spinal interbody fusion cage
BASE Ti HL Implant, 8x34x28mm 20°
Nuvasive, Inc.
6959011
In Commercial Distribution

  • 00887517702609 ()


  • Metallic spinal interbody fusion cage
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