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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 Conn+LS, 5-6/6.35mm O-H Rotate
Nuvasive, Inc.
12104060P
In Commercial Distribution

  • 00195377007476 ()


  • Bone-screw internal spinal fixation system, sterile
RSS Conn+LS, 60mm Offset Open
Nuvasive, Inc.
12111260P
In Commercial Distribution

  • 00195377007469 ()


  • Bone-screw internal spinal fixation system, sterile
RSS Conn+LS, 60mm Offset Closed
Nuvasive, Inc.
12111360P
In Commercial Distribution

  • 00195377007452 ()


  • Bone-screw internal spinal fixation system, sterile
RSS Lock Screw, Closed Tulip
Nuvasive, Inc.
13100000P
In Commercial Distribution

  • 00195377007445 ()


  • Bone-screw internal spinal fixation system, sterile
RSS Lock Screw, Closed Tulip/2PK
Nuvasive, Inc.
13100001P
In Commercial Distribution

  • 00195377007438 ()


  • Bone-screw internal spinal fixation system, sterile
RSS Lock Screw, 4.5-5.0mm
Nuvasive, Inc.
13450000P
In Commercial Distribution

  • 00195377007421 ()


  • Bone-screw internal spinal fixation system, sterile
RSS Lock Screw, 4.5-5.0mm/4PK
Nuvasive, Inc.
13450001P
In Commercial Distribution

  • 00195377007414 ()


  • Bone-screw internal spinal fixation system, sterile
RSS Screw+LS, 4.0x22.5mm Poly 2S
Nuvasive, Inc.
14414022P
In Commercial Distribution

  • 00195377007407 ()


  • Bone-screw internal spinal fixation system, sterile
RSS Screw+LS, 6.0x40mm Poly 2S
Nuvasive, Inc.
14416040P
In Commercial Distribution

  • 00195377007391 ()


  • Bone-screw internal spinal fixation system, sterile
RSS Screw+LS, 6.0x45mm Poly 2S
Nuvasive, Inc.
14416045P
In Commercial Distribution

  • 00195377007384 ()


  • Bone-screw internal spinal fixation system, sterile
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