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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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Trial 27Dx36Wx16H 20°
NEXXT SPINE, LLC
336H2016
In Commercial Distribution

  • 00840067204795 ()


  • General internal orthopaedic fixation system implantation kit
Trial 27Dx36Wx14H 20°
NEXXT SPINE, LLC
336H2014
In Commercial Distribution

  • 00840067204788 ()


  • General internal orthopaedic fixation system implantation kit
Trial 27Dx36Wx12H 20°
NEXXT SPINE, LLC
336H2012
In Commercial Distribution

  • 00840067204771 ()


  • General internal orthopaedic fixation system implantation kit
Trial 24Dx32Wx20H 20°
NEXXT SPINE, LLC
332H2020
In Commercial Distribution

  • 00840067204634 ()


  • General internal orthopaedic fixation system implantation kit
Trial 24Dx32Wx18H 20°
NEXXT SPINE, LLC
332H2018
In Commercial Distribution

  • 00840067204627 ()


  • General internal orthopaedic fixation system implantation kit
Trial 24Dx32Wx16H 20°
NEXXT SPINE, LLC
332H2016
In Commercial Distribution

  • 00840067204610 ()


  • General internal orthopaedic fixation system implantation kit
Trial 24Dx32Wx14H 20°
NEXXT SPINE, LLC
332H2014
In Commercial Distribution

  • 00840067204603 ()


  • General internal orthopaedic fixation system implantation kit
Trial 24Dx32Wx12H 20°
NEXXT SPINE, LLC
332H2012
In Commercial Distribution

  • 00840067204597 ()


  • General internal orthopaedic fixation system implantation kit
Curette, large, 20°
Karl Storz GmbH & Co. KG
28195KC
In Commercial Distribution

  • 04048551109069 ()


  • Bone curette, reusable
K-FILES 21MM #20
HENRY SCHEIN, INC.
1006180
In Commercial Distribution

  • H65810061809 ()
  • H65810061801 ()
1006180

  • Manual endodontic file/rasp, reusable
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