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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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RELINE MAS Screw, 11.0x35mm 2C Polyaxial
Nuvasive, Inc.
16011135
In Commercial Distribution

  • 00887517552136 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Screw, 11.0x30mm 2C Polyaxial
Nuvasive, Inc.
16011130
In Commercial Distribution

  • 00887517552129 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Screw, 11.0x25mm 2C Polyaxial
Nuvasive, Inc.
16011125
In Commercial Distribution

  • 00887517552112 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Screw,11.0x120mm 2C PolyIliac
Nuvasive, Inc.
16011112
In Commercial Distribution

  • 00887517552105 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Screw,11.0x110mm 2C PolyIliac
Nuvasive, Inc.
16011111
In Commercial Distribution

  • 00887517552099 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Screw,11.0x100mm 2C PolyIliac
Nuvasive, Inc.
16011110
In Commercial Distribution

  • 00887517552082 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Screw,10.0x95mm 2C Poly Iliac
Nuvasive, Inc.
16011095
In Commercial Distribution

  • 00887517552075 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Screw,10.0x90mm 2C Poly Iliac
Nuvasive, Inc.
16011090
In Commercial Distribution

  • 00887517552068 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Screw,10.0x85mm 2C Poly Iliac
Nuvasive, Inc.
16011085
In Commercial Distribution

  • 00887517552051 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Screw,10.0x80mm 2C Poly Iliac
Nuvasive, Inc.
16011080
In Commercial Distribution

  • 00887517552044 ()


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