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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
142M0007
In Commercial Distribution

  • 00880304838123 ()

  • Nerve Root Retractor 7 mm
142M0007

  • Self-retaining surgical retractor, reusable
No Description
BIOMET SPINE LLC
142M0006
In Commercial Distribution

  • 00880304838116 ()

  • Nerve Root Retractor 6 mm
142M0006

  • Self-retaining surgical retractor, reusable
No Description
BIOMET SPINE LLC
142M0005
In Commercial Distribution

  • 00880304838109 ()

  • Nerve Root Retractor 5 mm
142M0005

  • Self-retaining surgical retractor, reusable
No Description
BIOMET SPINE LLC
131M1003
In Commercial Distribution

  • 00880304836648 ()

  • Graft Tamp Angled
131M1003

  • Surgical tamp, reusable
No Description
BIOMET SPINE LLC
131M1002
In Commercial Distribution

  • 00880304836631 ()

  • Graft Tamp Straight
131M1002

  • Surgical tamp, reusable
No Description
BIOMET SPINE LLC
LV01220
In Commercial Distribution

  • 00880304826083 ()
LV01220

  • Orthopaedic inorganic implant inserter/extractor, reusable
No Description
BIOMET SPINE LLC
LV00531
In Commercial Distribution

  • 00888480499947 ()

  • LINEUM LOCKING SCREW INSERTER
LV00531

  • Orthopaedic inorganic implant inserter/extractor, reusable
No Description
BIOMET SPINE LLC
LV00492
In Commercial Distribution

  • 00888480499749 ()

  • EXTENDED SCREW INSERTER LINEUM
LV00492

  • Orthopaedic inorganic implant inserter/extractor, reusable
No Description
BIOMET SPINE LLC
07.01679.001
In Commercial Distribution

  • 00889024326422 ()

  • Compression Pin
07.01679.001

  • General surgical procedure kit, non-medicated, single-use
No Description
BIOMET SPINE LLC
07.01678.001
In Commercial Distribution

  • 00889024326415 ()

  • Fixation Pin
07.01678.001

  • General surgical procedure kit, non-medicated, single-use
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