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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Self Retaining Driver, Facet Screw
Life Spine, Inc.
144-023
In Commercial Distribution

  • 00190837041267 ()
144-023

  • Bone-screw internal spinal fixation system, non-sterile
Cannulated Drill, Facet Screw
Life Spine, Inc.
144-002
In Commercial Distribution

  • 00190837041182 ()
144-002

  • Bone-screw internal spinal fixation system, non-sterile
Facet Screw Driver, Short
Life Spine, Inc.
144-001
In Commercial Distribution

  • 00190837041175 ()
144-001

  • Bone-screw internal spinal fixation system, non-sterile
FS3 - Facet Screw System
Life Spine, Inc.
114-810
In Commercial Distribution

  • 00190837041120 ()
114-810

  • Bone-screw internal spinal fixation system, non-sterile
36kHz Manifold Tubing Set Sterile
KIRWAN SURGICAL PRODUCTS LLC
40-3601
In Commercial Distribution

  • 10841019107734 ()
  • 00841019107737 ()


  • Ultrasonic surgical system tubing set
23kHz Manifold Tubing Set Sterile
KIRWAN SURGICAL PRODUCTS LLC
40-3600
In Commercial Distribution

  • 10841019107727 ()
  • 00841019107720 ()


  • Ultrasonic surgical system tubing set
Washer (CP4) D10x5
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039825269 ()
FA.WC.1005

  • Bone-screw internal spinal fixation system, non-sterile
Washer D10x5
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039825252 ()
FA.WS.1005

  • Bone-screw internal spinal fixation system, non-sterile
Fenestrated Facet Screw Cannulated D5.5 x 60
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039825245 ()
FT.FC.5560

  • Bone-screw internal spinal fixation system, non-sterile
Fenestrated Facet Screw Cannulated D5.5 x 55
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039825238 ()
FT.FC.5555

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