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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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CoRoent® XL-CTW, 10x22x45mm, 10°
Nuvasive, Inc.
7221045
In Commercial Distribution

  • 00887517287175 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-CTW, 16x22x60mm
Nuvasive, Inc.
7211660
In Commercial Distribution

  • 00887517287151 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-CTW, 16x22x55mm
Nuvasive, Inc.
7211655
In Commercial Distribution

  • 00887517287144 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-CTW, 16x22x50mm
Nuvasive, Inc.
7211650
In Commercial Distribution

  • 00887517287137 ()


  • Polymeric spinal interbody fusion cage
CoRoent® XL-CTW, 16x22x45mm
Nuvasive, Inc.
7211645
In Commercial Distribution

  • 00887517287120 ()


  • Polymeric spinal interbody fusion cage
RELINE-O CoCr Rod, 5.0mm Lateral Off Med
Nuvasive, Inc.
18250002
In Commercial Distribution

  • 00887517287090 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 6.0mm Lateral Off Med
Nuvasive, Inc.
18160002
In Commercial Distribution

  • 00887517287083 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.5mm Lateral Off Med
Nuvasive, Inc.
18155002
In Commercial Distribution

  • 00887517287076 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Ti Rod, 5.0mm Lateral Off Med
Nuvasive, Inc.
18150002
In Commercial Distribution

  • 00887517287069 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O CpTi Rod, 6.0mm Lateral Off Med
Nuvasive, Inc.
18060002
In Commercial Distribution

  • 00887517287052 ()


  • Bone-screw internal spinal fixation system, non-sterile
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