SEARCH RESULTS FOR: (*Fake Texas A*)(32619 results)

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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 Type Device Class Implantable

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No Description
BIOMET SPINE LLC
55001909
In Commercial Distribution

  • 00888480360490 ()

  • C-THRU LORDOTIC 11X11X9MM
55001909

  • Polymeric spinal fusion cage, sterile
No Description
BIOMET SPINE LLC
55001908
In Commercial Distribution

  • 00888480360483 ()

  • C-THRU LORDOTIC 11X11X8MM
55001908

  • Polymeric spinal fusion cage, sterile
No Description
BIOMET SPINE LLC
55001907
In Commercial Distribution

  • 00888480360476 ()

  • C-THRU LORDOTIC 11X11X7MM
55001907

  • Polymeric spinal fusion cage, sterile
No Description
BIOMET SPINE LLC
55001906
In Commercial Distribution

  • 00888480360469 ()

  • C-THRU LORDOTIC 11X11X6MM
55001906

  • Polymeric spinal fusion cage, sterile
No Description
BIOMET SPINE LLC
55001905
In Commercial Distribution

  • 00888480360452 ()

  • C-THRU LORDOTIC 11X11X5MM
55001905

  • Polymeric spinal fusion cage, sterile
No Description
BIOMET SPINE LLC
1200-9232
In Commercial Distribution

  • 00888480145097 ()

  • CROSS CONNECTOR GUIDE
1200-9232

  • Orthopaedic implantation sleeve, reusable
No Description
BIOMET SPINE LLC
1861-1
In Commercial Distribution

  • 00889024331570 ()

  • Pituitary Rongeur - Bite (5 mm)
1861-1

  • Spinal rongeur
No Description
BIOMET SPINE LLC
1803-08
In Commercial Distribution

  • 00889024331150 ()

  • Endcap (8 mm)
1803-08

  • Metallic spinal fusion cage, non-sterile
No Description
BIOMET SPINE LLC
1050-12
In Commercial Distribution

  • 00889024330856 ()

  • Ring Curette, Angled #2
1050-12

  • Bone curette, reusable
No Description
BIOMET SPINE LLC
07.01777.001
In Commercial Distribution

  • 00889024329089 ()

  • Kerrison Rod Reducer
07.01777.001

  • General internal orthopaedic fixation system implantation kit
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