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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 Class Implantable

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RELINE-O Screw, 12.0x40mm 2S Polyaxial
Nuvasive, Inc.
13011240
In Commercial Distribution

  • 00887517535764 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.0x35mm 2S Polyaxial
Nuvasive, Inc.
13011235
In Commercial Distribution

  • 00887517535757 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.0x30mm 2S Polyaxial
Nuvasive, Inc.
13011230
In Commercial Distribution

  • 00887517535740 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.0x25mm 2S Polyaxial
Nuvasive, Inc.
13011225
In Commercial Distribution

  • 00887517535733 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.0x120mm 2S Poly Iliac
Nuvasive, Inc.
13011212
In Commercial Distribution

  • 00887517535726 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.0x110mm 2S Poly Iliac
Nuvasive, Inc.
13011211
In Commercial Distribution

  • 00887517535719 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.0x100mm 2S Poly Iliac
Nuvasive, Inc.
13011210
In Commercial Distribution

  • 00887517535702 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 11.0x95mm 2S Poly Iliac
Nuvasive, Inc.
13011195
In Commercial Distribution

  • 00887517535696 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 11.0x90mm 2S Poly Iliac
Nuvasive, Inc.
13011190
In Commercial Distribution

  • 00887517535689 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 11.0x85mm 2S Poly Iliac
Nuvasive, Inc.
13011185
In Commercial Distribution

  • 00887517535672 ()


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