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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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XLIF APX, 12x26x50mm 0°
Nuvasive, Inc.
1672379
In Commercial Distribution

  • 00887517453693 ()


  • Vertebral body prosthesis
XLIF APX, 10x26x50mm 0°
Nuvasive, Inc.
1672343
In Commercial Distribution

  • 00887517451590 ()


  • Vertebral body prosthesis
COHERE XLXW, 8x26x55mm 0°
Nuvasive, Inc.
8267855P2
In Commercial Distribution

  • 00887517984043 ()


  • Polymeric spinal interbody fusion cage
COHERE XLXW, 8x26x45mm 0°
Nuvasive, Inc.
8267845P2
In Commercial Distribution

  • 00887517984005 ()


  • Polymeric spinal interbody fusion cage
COHERE XLXW, 12x26x50mm 0°
Nuvasive, Inc.
8267250P2
In Commercial Distribution

  • 00887517983947 ()


  • Polymeric spinal interbody fusion cage
COHERE XLXW, 10x26x60mm 0°
Nuvasive, Inc.
8267160P2
In Commercial Distribution

  • 00887517983909 ()


  • Polymeric spinal interbody fusion cage
COHERE XLXW, 10x26x50mm 0°
Nuvasive, Inc.
8267150P2
In Commercial Distribution

  • 00887517983862 ()


  • Polymeric spinal interbody fusion cage
COHERE XLXW, 10x26x45mm 0°
Nuvasive, Inc.
8267145P2
In Commercial Distribution

  • 00887517983848 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 8x22x60mm 0°
Nuvasive, Inc.
8227860P2
In Commercial Distribution

  • 00887517983589 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 8x22x55mm 0°
Nuvasive, Inc.
8227855P2
In Commercial Distribution

  • 00887517983565 ()


  • Polymeric spinal interbody fusion cage
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