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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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18mm x 14mm W x 25mm L x 0 degrees XLIF
SUMMIT SPINE LLC
1
In Commercial Distribution

  • B587X1814250 ()

  • Width: 14 Millimeter
  • Length: 25 Millimeter
  • Height: 18 Millimeter
X181425

  • Polymeric spinal interbody fusion cage
ORIO-AL ALIF ANTERIOR LUMBAR, 0¿ LORDOSIS, 23 X 31 X20 mm
SPINECRAFT, LLC
A7100-20
In Commercial Distribution

  • M824A7100201 ()


  • Polymeric spinal interbody fusion cage
ORIO-AL ALIF ANTERIOR LUMBAR, 0¿ LORDOSIS, 23 X 31 X 18mm
SPINECRAFT, LLC
A7100-18
In Commercial Distribution

  • M824A7100181 ()


  • Polymeric spinal interbody fusion cage
ORIO-AL ALIF ANTERIOR LUMBAR, 0¿ LORDOSIS, 23 X 31 X 16mm
SPINECRAFT, LLC
A7100-16
In Commercial Distribution

  • M824A7100161 ()


  • Polymeric spinal interbody fusion cage
ORIO-AL ALIF ANTERIOR LUMBAR, 0¿ LORDOSIS, 23 X 3 1X 14mm
SPINECRAFT, LLC
A7100-14
In Commercial Distribution

  • M824A7100141 ()


  • Polymeric spinal interbody fusion cage
ORIO-AL ALIF ANTERIOR LUMBAR, 0¿ LORDOSIS, 23 X 31 X 12mm
SPINECRAFT, LLC
A7100-12
In Commercial Distribution

  • M824A7100121 ()


  • Polymeric spinal interbody fusion cage
ORIO-AL ALIF ANTERIOR LUMBAR, 0¿ LORDOSIS, 23 X 31 X 10mm
SPINECRAFT, LLC
A7100-10
In Commercial Distribution

  • M824A7100101 ()


  • Polymeric spinal interbody fusion cage
ORIO-AL ALIF ANTERIOR LUMBAR, 0¿ LORDOSIS, 27 X 35 X 20mm
SPINECRAFT, LLC
A7200-20
In Commercial Distribution

  • M824A7200201 ()


  • Polymeric spinal interbody fusion cage
ORIO-AL ALIF ANTERIOR LUMBAR, 0¿ LORDOSIS, 27 X 35 X 18mm
SPINECRAFT, LLC
A7200-18
In Commercial Distribution

  • M824A7200181 ()


  • Polymeric spinal interbody fusion cage
ORIO-AL ALIF ANTERIOR LUMBAR, 0¿ LORDOSIS, 27 X 35 X 16mm
SPINECRAFT, LLC
A7200-16
In Commercial Distribution

  • M824A7200161 ()


  • Polymeric spinal interbody fusion cage
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