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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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TI SPIRAL BLD 65MM-STER F/TI RETROGRADE FEMORAL NAILS-EX
Synthes GmbH
04.013.045S
In Commercial Distribution

  • H67904013045S0 ()
  • 10886982087454 ()
04013045S

  • Spiral blade
TI SPIRAL BLD 60MM-STER F/TI RETROGRADE FEMORAL NAILS-EX
Synthes GmbH
04.013.044S
In Commercial Distribution

  • H67904013044S0 ()
  • 10886982087430 ()
04013044S

  • Spiral blade
TI SPIRAL BLD 55MM-STER F/TI RETROGRADE FEMORAL NAILS-EX
Synthes GmbH
04.013.043S
In Commercial Distribution

  • H67904013043S0 ()
  • 10886982087416 ()
04013043S

  • Spiral blade
TI SPIRAL BLD 50MM-STER F/TI RETROGRADE FEMORAL NAILS-EX
Synthes GmbH
04.013.042S
In Commercial Distribution

  • H67904013042S0 ()
  • 10886982087393 ()
04013042S

  • Spiral blade
TI SPIRAL BLD 45MM-STER F/TI RETROGRADE FEMORAL NAILS-EX
Synthes GmbH
04.013.041S
In Commercial Distribution

  • H67904013041S0 ()
  • 10886982087379 ()
04013041S

  • Spiral blade
SONICPIN RX, PDLLA
KLS-Martin L.P.
52-621-25-04
In Commercial Distribution

  • 10888118001280 ()
  • 00888118001283 ()

  • 2.1 X 5 MM


  • Craniofacial bone tack, bioabsorbable
SONICPIN RX, PDLLA
KLS-Martin L.P.
52-621-24-04
In Commercial Distribution

  • 10888118001273 ()
  • 00888118001276 ()

  • 2.1 X 4 MM


  • Craniofacial bone tack, bioabsorbable
SONICPIN RX, PDLLA
KLS-Martin L.P.
52-616-24-04
In Commercial Distribution

  • 10888118001266 ()
  • 00888118001269 ()

  • 1.6 X 4 MM


  • Craniofacial bone tack, bioabsorbable
SONICPIN RXG, PLLA-PGA
KLS-Martin L.P.
52-522-57-04
In Commercial Distribution

  • 10888118001259 ()
  • 00888118001252 ()

  • 2.1 X 7 MM


  • Craniofacial bone tack, bioabsorbable
SONICPIN RXG, PLLA-PGA
KLS-Martin L.P.
52-522-56-04
In Commercial Distribution

  • 10888118001242 ()
  • 00888118001245 ()

  • 2.1 X 6 MM


  • Craniofacial bone tack, bioabsorbable
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