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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 Class Implantable

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RSS Ti Rod, 4.5x500mm Straight
Nuvasive, Inc.
20345500P
In Commercial Distribution

  • 00195377006844 ()


  • Bone-screw internal spinal fixation system, sterile
RSS CoCr Rod, 4.5x300mm Straight
Nuvasive, Inc.
20445300P
In Commercial Distribution

  • 00195377006837 ()


  • Bone-screw internal spinal fixation system, sterile
RSS CoCr Rod, 4.5x500mm Straight
Nuvasive, Inc.
20445500P
In Commercial Distribution

  • 00195377006820 ()


  • Bone-screw internal spinal fixation system, sterile
COHERE Cervical, 6x14x12mm 7°
Nuvasive, Inc.
4061427P2
In Commercial Distribution

  • 00195377006813 ()


  • Polymeric spinal interbody fusion cage
COHERE Cervical, 6x16x14mm 7°
Nuvasive, Inc.
4061647P2
In Commercial Distribution

  • 00195377006806 ()


  • Polymeric spinal interbody fusion cage
COHERE Cervical, 7x14x12mm 7°
Nuvasive, Inc.
4071427P2
In Commercial Distribution

  • 00195377006790 ()


  • Polymeric spinal interbody fusion cage
COHERE Cervical, 7x16x14mm 7°
Nuvasive, Inc.
4071647P2
In Commercial Distribution

  • 00195377006783 ()


  • Polymeric spinal interbody fusion cage
COALESCE Straight, 8x10x28mm 8°
Nuvasive, Inc.
4080288P2
In Commercial Distribution

  • 00195377006776 ()


  • Polymeric spinal interbody fusion cage
COHERE Cervical, 8x14x12mm 7°
Nuvasive, Inc.
4081427P2
In Commercial Distribution

  • 00195377006769 ()


  • Polymeric spinal interbody fusion cage
COHERE Cervical, 9x14x12mm 7°
Nuvasive, Inc.
4091427P2
In Commercial Distribution

  • 00195377006752 ()


  • Polymeric spinal interbody fusion cage
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