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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
14-520508
In Commercial Distribution

  • 00880304908802 ()

  • Spacer 8H x 14W x 12D-L PEEK Lordotic (7°)
14-520508

  • Vertebral body prosthesis
No Description
BIOMET SPINE LLC
14-520507
In Commercial Distribution

  • 00880304908796 ()

  • Spacer 7H x 14W x 12D-L PEEK Lordotic (7°)
14-520507

  • Vertebral body prosthesis
No Description
BIOMET SPINE LLC
14-520506
In Commercial Distribution

  • 00880304908789 ()

  • Spacer 6H x 14W x 12D-L PEEK Lordotic (7°)
14-520506

  • Vertebral body prosthesis
No Description
BIOMET SPINE LLC
104M3315
In Commercial Distribution

  • 00880304864580 ()

  • Curved Titanium Spacer Lordotic 33L x 15H x 11W 10°
104M3315

  • Spinal implant trial
No Description
BIOMET SPINE LLC
104M3314
In Commercial Distribution

  • 00880304864573 ()

  • Curved Titanium Spacer Lordotic 33L x 14H x 11W 10°
104M3314

  • Spinal implant trial
No Description
BIOMET SPINE LLC
104M3313
In Commercial Distribution

  • 00880304864566 ()

  • Curved Titanium Spacer Lordotic 33L x 13H x 11W 10°
104M3313

  • Spinal implant trial
No Description
BIOMET SPINE LLC
104M3312
In Commercial Distribution

  • 00880304864559 ()

  • Curved Titanium Spacer Lordotic 33L x 12H x 10W 10°
104M3312

  • Spinal implant trial
No Description
BIOMET SPINE LLC
104M3311
In Commercial Distribution

  • 00880304864542 ()

  • Curved Titanium Spacer Lordotic 33L x 11H x 10W 10°
104M3311

  • Spinal implant trial
No Description
BIOMET SPINE LLC
104M3310
In Commercial Distribution

  • 00880304864535 ()

  • Curved Titanium Spacer Lordotic 33L x 10H x 10W 10°
104M3310

  • Spinal implant trial
No Description
BIOMET SPINE LLC
104M3309
In Commercial Distribution

  • 00880304864528 ()

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

  • Spinal implant trial
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