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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
8409-2105
In Commercial Distribution

  • 00887868193293 ()

  • Half-Plate Caudal Ti 5mm
8409-2105

  • Bone-screw internal spinal fixation system, non-sterile
No Description
BIOMET SPINE LLC
8409-1212
In Commercial Distribution

  • 00887868193286 ()

  • Full-Plate Ti 10° 12mm
8409-1212

  • Bone-screw internal spinal fixation system, non-sterile
No Description
BIOMET SPINE LLC
8409-1211
In Commercial Distribution

  • 00887868193279 ()

  • Full-Plate Ti 10° 11mm
8409-1211

  • Bone-screw internal spinal fixation system, non-sterile
No Description
BIOMET SPINE LLC
8409-1210
In Commercial Distribution

  • 00887868193262 ()

  • Full-Plate Ti 10° 10mm
8409-1210

  • Bone-screw internal spinal fixation system, non-sterile
No Description
BIOMET SPINE LLC
8409-1209
In Commercial Distribution

  • 00887868193255 ()

  • Full-Plate Ti 10° 9mm
8409-1209

  • Bone-screw internal spinal fixation system, non-sterile
No Description
BIOMET SPINE LLC
8409-1208
In Commercial Distribution

  • 00887868193248 ()

  • Full-Plate Ti 10° 8mm
8409-1208

  • Bone-screw internal spinal fixation system, non-sterile
No Description
BIOMET SPINE LLC
8409-1207
In Commercial Distribution

  • 00887868193231 ()

  • Full-Plate Ti 10° 7mm
8409-1207

  • Bone-screw internal spinal fixation system, non-sterile
No Description
BIOMET SPINE LLC
8409-1206
In Commercial Distribution

  • 00887868193224 ()

  • Full-Plate Ti 10° 6mm
8409-1206

  • Bone-screw internal spinal fixation system, non-sterile
No Description
BIOMET SPINE LLC
8409-1205
In Commercial Distribution

  • 00887868193217 ()

  • Full-Plate Ti 10° 5mm
8409-1205

  • Bone-screw internal spinal fixation system, non-sterile
No Description
BIOMET SPINE LLC
8409-1112
In Commercial Distribution

  • 00887868193200 ()

  • Half-Plate Cranial Ti 12mm
8409-1112

  • Bone-screw internal spinal fixation system, non-sterile
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