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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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PGI - 00887517938800

PGI II Pituitary, 2mm Bayoneted Str
Nuvasive, Inc.
1667772
In Commercial Distribution

  • 00887517938800 ()


  • Orthopaedic joint/limb rongeur

PGI - 00887517938794

PGI II Kerrison, 5mm 40° Bayoneted
Nuvasive, Inc.
1667755
In Commercial Distribution

  • 00887517938794 ()


  • Orthopaedic joint/limb rongeur

PGI - 00887517938787

PGI II Kerrison, 4mm 40° Bayoneted
Nuvasive, Inc.
1667754
In Commercial Distribution

  • 00887517938787 ()


  • Orthopaedic joint/limb rongeur

PGI - 00887517938770

PGI II Kerrison, 3mm 40° Bayoneted
Nuvasive, Inc.
1667753
In Commercial Distribution

  • 00887517938770 ()


  • Orthopaedic joint/limb rongeur

PGI - 00887517938763

PGI II Kerrison, 2mm 40° Bayoneted
Nuvasive, Inc.
1667752
In Commercial Distribution

  • 00887517938763 ()


  • Orthopaedic joint/limb rongeur

PGI - 00887517938756

PGI II Lamina Spreader
Nuvasive, Inc.
1667750
In Commercial Distribution

  • 00887517938756 ()


  • Bone distraction forceps

PGI - 00887517938749

PGI II Rasp, Bayoneted Right Angled
Nuvasive, Inc.
1667745
In Commercial Distribution

  • 00887517938749 ()


  • Bone file/rasp, manual, reusable

PGI - 00887517938732

PGI II Rasp, Bayoneted Straight
Nuvasive, Inc.
1667740
In Commercial Distribution

  • 00887517938732 ()


  • Bone file/rasp, manual, reusable

PGI - 00887517938619

PGI II Slap Hammer
Nuvasive, Inc.
1667700
In Commercial Distribution

  • 00887517938619 ()


  • Internal spinal fixation procedure kit, reusable

PGI - 00887517938602

PGI II Curette, Large Right
Nuvasive, Inc.
1667699
In Commercial Distribution

  • 00887517938602 ()


  • Neurosurgical curette, single-use
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