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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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FOOT KINETIC LIGHT RT 22 #1 DK BRN
TRULIFE LIMITED
SKF103-22-R-1A2
In Commercial Distribution

  • 00645517841014 ()


  • Mechanical-resistance external ankle-foot prosthesis
FOOT KINETIC LIGHT LFT 22 #1 DK BRN
TRULIFE LIMITED
SKF103-22-L-1A2
In Commercial Distribution

  • 00645517840963 ()


  • Mechanical-resistance external ankle-foot prosthesis
FOOT KINETIC LIGHT RT 30 #5
TRULIFE LIMITED
SKF100-30-R-5B0
In Commercial Distribution

  • 00645517840055 ()


  • Mechanical-resistance external ankle-foot prosthesis
FOOT KINETIC LIGHT RT 30 #4
TRULIFE LIMITED
SKF100-30-R-4B0
In Commercial Distribution

  • 00645517840048 ()


  • Mechanical-resistance external ankle-foot prosthesis
FOOT KINETIC LIGHT LFT 30 #5
TRULIFE LIMITED
SKF100-30-L-5B0
In Commercial Distribution

  • 00645517840000 ()


  • Mechanical-resistance external ankle-foot prosthesis
FOOT KINETIC LIGHT LFT 30 #4
TRULIFE LIMITED
SKF100-30-L-4B0
In Commercial Distribution

  • 00645517839998 ()


  • Mechanical-resistance external ankle-foot prosthesis
FOOT KINETIC LIGHT RT 29 #5
TRULIFE LIMITED
SKF100-29-R-5B9
In Commercial Distribution

  • 00645517839950 ()


  • Mechanical-resistance external ankle-foot prosthesis
FOOT KINETIC LIGHT RT 29 #4
TRULIFE LIMITED
SKF100-29-R-4B9
In Commercial Distribution

  • 00645517839943 ()


  • Mechanical-resistance external ankle-foot prosthesis
FOOT KINETIC LIGHT RT 29 #3
TRULIFE LIMITED
SKF100-29-R-3B9
In Commercial Distribution

  • 00645517839936 ()


  • Mechanical-resistance external ankle-foot prosthesis
FOOT KINETIC LIGHT LFT 29 #5
TRULIFE LIMITED
SKF100-29-L-5B9
In Commercial Distribution

  • 00645517839905 ()


  • Mechanical-resistance external ankle-foot prosthesis
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