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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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PTA, RX, 2.5 x 20, 200cm
CORDIS CORPORATION
47525020L
In Commercial Distribution

  • 20705032089675 ()
47525020L

  • Peripheral angioplasty balloon catheter, basic
PTA, RX, 2.5 x 20, 150cm
CORDIS CORPORATION
47525020M
In Commercial Distribution

  • 20705032089644 ()
47525020M

  • Peripheral angioplasty balloon catheter, basic
PTA, RX, 2.0 x 20, 150cm
CORDIS CORPORATION
47520020M
In Commercial Distribution

  • 20705032089538 ()
47520020M

  • Peripheral angioplasty balloon catheter, basic
PTA, RX, 2.0 x 20, 200cm
CORDIS CORPORATION
47520020L
In Commercial Distribution

  • 20705032089514 ()
47520020L

  • Peripheral angioplasty balloon catheter, basic
PTA, RX, 2.0 x 20, 90cm
CORDIS CORPORATION
47520020S
In Commercial Distribution

  • 20705032089484 ()
47520020S

  • Peripheral angioplasty balloon catheter, basic
PTA, OTW, 4.0 x 20, 90cm
CORDIS CORPORATION
47040020S
In Commercial Distribution

  • 20705032089460 ()
47040020S

  • Peripheral angioplasty balloon catheter, basic
Vitriguard Green - 20 pouches per box
Origio A/S
43802001
In Commercial Distribution

  • 20888937014819 ()
  • 00888937014815 ()


  • Assisted reproduction vitrification carrier
VitriGuard Blue - 20 pouches per box
Origio A/S
43792001
In Commercial Distribution

  • 20888937014802 ()
  • 00888937014808 ()


  • Assisted reproduction vitrification carrier
VitriGuard Clear - 20 pouches per box
Origio A/S
43782001
In Commercial Distribution

  • 20888937014796 ()
  • 00888937014792 ()


  • Assisted reproduction vitrification carrier
BI-OK Steam Test-Pak w/ 20 Controls
PROPPER MANUFACTURING COMPANY, INC.
26922000
In Commercial Distribution

  • 70818087012392 ()
  • 10818087012390 ()


  • Biological sterilization indicator
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