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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 Type Device Class Implantable

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No Description
BIOMET SPINE LLC
104M3309
In Commercial Distribution

  • 00880304864528 ()

  • Curved Titanium Spacer Lordotic 33L x 09H x 10W 10°
104M3309

  • Spinal implant trial
No Description
BIOMET SPINE LLC
104M3308
In Commercial Distribution

  • 00880304864511 ()

  • Curved Titanium Spacer Lordotic 33L x 08H x 10W 10°
104M3308

  • Spinal implant trial
No Description
BIOMET SPINE LLC
104M2815
In Commercial Distribution

  • 00880304864481 ()

  • Curved Titanium Spacer Lordotic 28L x 15H x 11W 10°
104M2815

  • Spinal implant trial
No Description
BIOMET SPINE LLC
104M2812
In Commercial Distribution

  • 00880304864450 ()

  • Curved Titanium Spacer Lordotic 28L x 12H x 10W 10°
104M2812

  • Spinal implant trial
No Description
BIOMET SPINE LLC
104M2810
In Commercial Distribution

  • 00880304864436 ()

  • Curved Titanium Spacer Lordotic 28L x 10H x 10W 10°
104M2810

  • Spinal implant trial
No Description
BIOMET SPINE LLC
104M2808
In Commercial Distribution

  • 00880304864412 ()

  • Curved Titanium Spacer Lordotic 28L x 08H x 10W 10°
104M2808

  • Spinal implant trial
No Description
BIOMET SPINE LLC
103M2614
In Commercial Distribution

  • 00880304864306 ()

  • Straight Titanium Spacer Lordotic 26L x 14H x 11W 10°
103M2614

  • Spinal implant trial
No Description
BIOMET SPINE LLC
103M2611
In Commercial Distribution

  • 00880304864276 ()

  • Straight Titanium Spacer Lordotic 26L x 11H x 10W 10°
103M2611

  • Spinal implant trial
No Description
BIOMET SPINE LLC
103M2610
In Commercial Distribution

  • 00880304864269 ()

  • Straight Titanium Spacer Lordotic 26L x 10H x 10W 10°
103M2610

  • Spinal implant trial
No Description
BIOMET SPINE LLC
103M2609
In Commercial Distribution

  • 00880304864252 ()

  • Straight Titanium Spacer Lordotic 26L x 09H x 10W 10°
103M2609

  • Spinal implant trial
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