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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
8732-6106
In Commercial Distribution

  • 00888480661054 ()

  • INSERTER IMPLANT
8732-6106

  • Orthopaedic inorganic implant inserter/extractor, reusable
No Description
BIOMET SPINE LLC
8732-6102
In Commercial Distribution

  • 00888480661016 ()

  • IMPLANT REMOVER
8732-6102

  • Orthopaedic inorganic implant inserter/extractor, reusable
No Description
BIOMET SPINE LLC
8732-2520
In Commercial Distribution

  • 00888480659457 ()

  • TRIAL IMPLANT LATERAL 0DEG 26 X 20
8732-2520

  • Spinal implant trial
No Description
BIOMET SPINE LLC
8732-2516
In Commercial Distribution

  • 00888480659433 ()

  • TRIAL IMPLANT LATERAL 0DEG 26 X 16
8732-2516

  • Spinal implant trial
No Description
BIOMET SPINE LLC
8732-1220
In Commercial Distribution

  • 00888480659006 ()

  • TRIAL IMPLANT LATERAL 8DEG 18 X 20DEG
8732-1220

  • Spinal implant trial
No Description
BIOMET SPINE LLC
8732-1216
In Commercial Distribution

  • 00888480658986 ()

  • TRIAL IMPLANT LATERAL 8DEG 18 X 16
8732-1216

  • Spinal implant trial
No Description
BIOMET SPINE LLC
8732-1214
In Commercial Distribution

  • 00888480658979 ()

  • TRIAL IMPLANT LATERAL 8DEG 18 X 14
8732-1214

  • Spinal implant trial
No Description
BIOMET SPINE LLC
8417-0712
In Commercial Distribution

  • 00888480556176 ()

  • ACDF PEEK 7° 12X15X12MM
8417-0712

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8417-0711
In Commercial Distribution

  • 00888480556169 ()

  • ACDF PEEK 7° 12X15X11MM
8417-0711

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8417-0710
In Commercial Distribution

  • 00888480556152 ()

  • ACDF PEEK 7° 12X15X10MM
8417-0710

  • Polymeric spinal interbody fusion cage
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