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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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RELINE MAS Screw, 7.5x95mm 2C Poly Iliac
Nuvasive, Inc.
16017595
In Commercial Distribution

  • 00887517554048 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Screw, 7.5x90mm 2C Poly Iliac
Nuvasive, Inc.
16017590
In Commercial Distribution

  • 00887517554031 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Screw, 7.5x85mm 2C Poly Iliac
Nuvasive, Inc.
16017585
In Commercial Distribution

  • 00887517554024 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Screw, 7.5x80mm 2C Poly Iliac
Nuvasive, Inc.
16017580
In Commercial Distribution

  • 00887517554017 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Screw, 7.5x75mm 2C Poly Iliac
Nuvasive, Inc.
16017575
In Commercial Distribution

  • 00887517554000 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Screw, 7.5x70mm 2C Poly Iliac
Nuvasive, Inc.
16017570
In Commercial Distribution

  • 00887517553997 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Screw, 7.5x65mm 2C Poly Iliac
Nuvasive, Inc.
16017565
In Commercial Distribution

  • 00887517553980 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Screw, 7.5x60mm 2C Poly Iliac
Nuvasive, Inc.
16017560
In Commercial Distribution

  • 00887517553973 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Screw, 7.5x55mm 2C Polyaxial
Nuvasive, Inc.
16017555
In Commercial Distribution

  • 00887517553966 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Screw, 7.5x50mm 2C Polyaxial
Nuvasive, Inc.
16017550
In Commercial Distribution

  • 00887517553959 ()


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