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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, 12x22x60mm 0°
Nuvasive, Inc.
8227260P2
In Commercial Distribution

  • 00887517983503 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 12x22x55mm 0°
Nuvasive, Inc.
8227255P2
In Commercial Distribution

  • 00887517983480 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 12x22x50mm 0°
Nuvasive, Inc.
8227250P2
In Commercial Distribution

  • 00887517983466 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 12x22x45mm 0°
Nuvasive, Inc.
8227245P2
In Commercial Distribution

  • 00887517983442 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 10x22x60mm 0°
Nuvasive, Inc.
8227160P2
In Commercial Distribution

  • 00887517983428 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 10x22x55mm 0°
Nuvasive, Inc.
8227155P2
In Commercial Distribution

  • 00887517983404 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 10x22x50mm 0°
Nuvasive, Inc.
8227150P2
In Commercial Distribution

  • 00887517983381 ()


  • Polymeric spinal interbody fusion cage
COHERE XLW, 10x22x45mm 0°
Nuvasive, Inc.
8227145P2
In Commercial Distribution

  • 00887517983367 ()


  • 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
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