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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 SHELL SEF 25 LT K34
TRULIFE LIMITED
SFC190-25-L-K34
In Commercial Distribution

  • 00645517821566 ()


  • Mechanical-resistance external ankle-foot prosthesis
FOOT SHELL SEF 24 RT K34
TRULIFE LIMITED
SFC190-24-R-K34
In Commercial Distribution

  • 00645517821559 ()


  • Mechanical-resistance external ankle-foot prosthesis
FOOT SHELL SEF 24 LT K34
TRULIFE LIMITED
SFC190-24-L-K34
In Commercial Distribution

  • 00645517821542 ()


  • Mechanical-resistance external ankle-foot prosthesis
FOOT SHELL SEF 23 RT K34
TRULIFE LIMITED
SFC190-23-R-K34
In Commercial Distribution

  • 00645517821535 ()


  • Mechanical-resistance external ankle-foot prosthesis
FOOT SHELL SEF 23 LT K34
TRULIFE LIMITED
SFC190-23-L-K34
In Commercial Distribution

  • 00645517821528 ()


  • Mechanical-resistance external ankle-foot prosthesis
FOOT SHELL SEF 22 RT K34
TRULIFE LIMITED
SFC190-22-R-K34
In Commercial Distribution

  • 00645517821511 ()


  • Mechanical-resistance external ankle-foot prosthesis
FOOT SHELL SEF 22 LT K34
TRULIFE LIMITED
SFC190-22-L-K34
In Commercial Distribution

  • 00645517821504 ()


  • Mechanical-resistance external ankle-foot prosthesis
FOOT SHELL SEF DK BRN 30 RT K12
TRULIFE LIMITED
SFC193-30-R-K12
In Commercial Distribution

  • 00645517821498 ()


  • Mechanical-resistance external ankle-foot prosthesis
FOOT SHELL SEF DK BRN 30 LT K12
TRULIFE LIMITED
SFC193-30-L-K12
In Commercial Distribution

  • 00645517821481 ()


  • Mechanical-resistance external ankle-foot prosthesis
FOOT SHELL SEF DK BRN 29 RT K12
TRULIFE LIMITED
SFC193-29-R-K12
In Commercial Distribution

  • 00645517821474 ()


  • Mechanical-resistance external ankle-foot prosthesis
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