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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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Full Handle Backflush 20G Standard Active/Passive
AKTIVE SRL
AK-0451/AP
In Commercial Distribution

  • 08056477557372 ()
  • 08052276026392 ()

  • GAUGE
AK-0451/AP

  • Vitrectomy fluid/gas handling handpiece/cannula
Active Reservoir
AKTIVE SRL
AK-0441
In Commercial Distribution

  • 08058340220741 ()
  • 08052276026385 ()

  • GAUGE
AK-0441

  • Vitrectomy fluid/gas handling handpiece/cannula
Passive Reservoir
AKTIVE SRL
AK-0440
In Commercial Distribution

  • 08058340220734 ()
  • 08052276026378 ()

  • GAUGE
AK-0440

  • Vitrectomy fluid/gas handling handpiece/cannula
No Description
TRIREME MEDICAL, LLC
D
In Commercial Distribution

  • M874CF1413525040OTW1 ()


  • Peripheral angioplasty balloon catheter, basic
No Description
TRIREME MEDICAL, LLC
D
In Commercial Distribution

  • M874CF1413525020OTW1 ()


  • Peripheral angioplasty balloon catheter, basic
No Description
TRIREME MEDICAL, LLC
B
In Commercial Distribution

  • M874CB1812060120OTW1 ()


  • Peripheral angioplasty balloon catheter, basic
No Description
TRIREME MEDICAL, LLC
B
In Commercial Distribution

  • M874CB1812060080OTW1 ()


  • Peripheral angioplasty balloon catheter, basic
No Description
TRIREME MEDICAL, LLC
B
In Commercial Distribution

  • M874CB1812060040OTW1 ()


  • Peripheral angioplasty balloon catheter, basic
No Description
TRIREME MEDICAL, LLC
B
In Commercial Distribution

  • M874CB1812060020OTW1 ()


  • Peripheral angioplasty balloon catheter, basic
No Description
TRIREME MEDICAL, LLC
B
In Commercial Distribution

  • M874CB1812055120OTW1 ()


  • Peripheral angioplasty balloon catheter, basic
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