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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 Size Type Device Class Implantable

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MEDITECH SPINE, LLC
515-120100
In Commercial Distribution

  • B1675151201000 ()


  • General internal orthopaedic fixation system implantation kit
PILOT POINT #13
ONKOS SURGICAL, INC.
20040113E
In Commercial Distribution

  • B27820040113E0 ()
20040113E

  • General internal orthopaedic fixation system implantation kit
PILOT POINT #12
ONKOS SURGICAL, INC.
20040112E
In Commercial Distribution

  • B27820040112E0 ()
20040112E

  • General internal orthopaedic fixation system implantation kit
PILOT POINT #11
ONKOS SURGICAL, INC.
20040111E
In Commercial Distribution

  • B27820040111E0 ()
20040111E

  • General internal orthopaedic fixation system implantation kit
PILOT POINT #10
ONKOS SURGICAL, INC.
20040110E
In Commercial Distribution

  • B27820040110E0 ()
20040110E

  • General internal orthopaedic fixation system implantation kit
RESURFACING PATELLA RESECTION GUIDE
ONKOS SURGICAL, INC.
18810220E
In Commercial Distribution

  • B27818810220E0 ()
18810220E

  • General internal orthopaedic fixation system implantation kit
SCREWDRIVER
ONKOS SURGICAL, INC.
18410135E
In Commercial Distribution

  • B27818410135E0 ()
18410135E

  • General internal orthopaedic fixation system implantation kit
TRIAL FEMORAL HEAD 32MM OD W/FLAT, +7MM
ONKOS SURGICAL, INC.
18056063E
In Commercial Distribution

  • B27818056063E0 ()
18056063E

  • General internal orthopaedic fixation system implantation kit
TRIAL FEMORAL HEAD 32MM OD W/FLAT, +0MM
ONKOS SURGICAL, INC.
18056061E
In Commercial Distribution

  • B27818056061E0 ()
18056061E

  • General internal orthopaedic fixation system implantation kit
TRIAL FEMORAL HEAD 28MM OD W/ FLAT +10MM
ONKOS SURGICAL, INC.
18056054E
In Commercial Distribution

  • B27818056054E0 ()
18056054E

  • General internal orthopaedic fixation system implantation kit
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