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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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MaXcess-C Blade, 19x40mm Blunt
Nuvasive, Inc.
1576052
In Commercial Distribution

  • 00887517083005 ()


  • Surgical retraction system, reusable
Helix Screw, Ø4.0x18mm Blunt Variable
Nuvasive, Inc.
7731218
In Commercial Distribution

  • 00887517082930 ()


  • Spinal fixation plate, non-bioabsorbable
Helix Screw, Ø4.0x16mm Blunt Variable
Nuvasive, Inc.
7731216
In Commercial Distribution

  • 00887517082916 ()


  • Spinal fixation plate, non-bioabsorbable
MaXcess-C Blade, 19x50mm Serrated
Nuvasive, Inc.
1576043
In Commercial Distribution

  • 00887517082695 ()


  • Surgical retraction system, reusable
MaXcess-C Blade, 19x30mm Serrated
Nuvasive, Inc.
1576041
In Commercial Distribution

  • 00887517082688 ()


  • Surgical retraction system, reusable
MaXcess-C Blade, 14x50mm Blunt
Nuvasive, Inc.
1576033
In Commercial Distribution

  • 00887517082671 ()


  • Surgical retraction system, reusable
MaXcess-C Blade, 14x30mm Blunt
Nuvasive, Inc.
1576031
In Commercial Distribution

  • 00887517082664 ()


  • Surgical retraction system, reusable
PCM Cervical Disc Instrument Tray, Middle
Nuvasive, Inc.
7690012
In Commercial Distribution

  • 00887517082596 ()


  • Orthopaedic surgical procedure kit, non-medicated, reusable
PCM Cervical Disc Instrument Tray, Top
Nuvasive, Inc.
7690011
In Commercial Distribution

  • 00887517082589 ()


  • Orthopaedic surgical procedure kit, non-medicated, reusable
PCM Cervical Disc Instrument Case Lid
Nuvasive, Inc.
7690002
In Commercial Distribution

  • 00887517082572 ()


  • Orthopaedic surgical procedure kit, non-medicated, reusable
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