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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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Interlock HL, 10x17x14mm 10°
Nuvasive, Inc.
1662312
In Commercial Distribution

  • 00887517711533 ()


  • Polymeric spinal interbody fusion cage
Interlock HL, 6x17x14mm 10°
Nuvasive, Inc.
1662302
In Commercial Distribution

  • 00887517711236 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL, 16x18x50mm 10°
Nuvasive, Inc.
6981650P2
In Commercial Distribution

  • 00887517708991 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL, 14x18x60mm 10°
Nuvasive, Inc.
6981460P2
In Commercial Distribution

  • 00887517708960 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL, 14x18x45mm 10°
Nuvasive, Inc.
6981445P2
In Commercial Distribution

  • 00887517708939 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL, 14x18x40mm 10°
Nuvasive, Inc.
6981440P2
In Commercial Distribution

  • 00887517708922 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL, 12x18x55mm 10°
Nuvasive, Inc.
6981255P2
In Commercial Distribution

  • 00887517708908 ()


  • Polymeric spinal interbody fusion cage
CoRoent XL, 12x18x45mm 10°
Nuvasive, Inc.
6981245P2
In Commercial Distribution

  • 00887517708885 ()


  • Polymeric spinal interbody fusion cage
Interlock HL, 9x17x14mm 10°
Nuvasive, Inc.
1662308
In Commercial Distribution

  • 00887517711298 ()


  • Polymeric spinal interbody fusion cage
Interlock HL, 8x17x14mm 10°
Nuvasive, Inc.
1662305
In Commercial Distribution

  • 00887517711267 ()


  • Polymeric spinal interbody fusion cage
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