SEARCH RESULTS FOR: (*Buy Two Internal Territory Driver*)(981763 results)

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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 Device Size Type Device Class Implantable

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VUELOCK® ANTERIOR CERVICAL PLATE SYSTEM - 00880304978928

No Description
BIOMET SPINE LLC
83258
In Commercial Distribution

  • 00880304978928 ()

  • TWO LEVEL 58MM PLATE
83258

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

VUELOCK® ANTERIOR CERVICAL PLATE SYSTEM - 00880304978911

No Description
BIOMET SPINE LLC
83260
In Commercial Distribution

  • 00880304978911 ()

  • TWO LEVEL 60MM PLATE
83260

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

VUELOCK® ANTERIOR CERVICAL PLATE SYSTEM - 00880304978904

No Description
BIOMET SPINE LLC
83262
In Commercial Distribution

  • 00880304978904 ()

  • TWO LEVEL 62MM PLATE
83262

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

VUELOCK® ANTERIOR CERVICAL PLATE SYSTEM - 00880304978898

No Description
BIOMET SPINE LLC
83264
In Commercial Distribution

  • 00880304978898 ()

  • TWO LEVEL 64MM PLATE
83264

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

VUELOCK® ANTERIOR CERVICAL PLATE SYSTEM - 00880304978881

No Description
BIOMET SPINE LLC
83266
In Commercial Distribution

  • 00880304978881 ()

  • TWO LEVEL 66MM PLATE
83266

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

VUELOCK® ANTERIOR CERVICAL PLATE SYSTEM - 00880304978874

No Description
BIOMET SPINE LLC
83268
In Commercial Distribution

  • 00880304978874 ()

  • TWO LEVEL 68MM PLATE
83268

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

VUELOCK® ANTERIOR CERVICAL PLATE SYSTEM - 00880304978867

No Description
BIOMET SPINE LLC
83270
In Commercial Distribution

  • 00880304978867 ()

  • TWO LEVEL 70MM PLATE
83270

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

Bioseal Inc. - 00630094194110

BIG O Sponge GREEN
BIOSEAL
19411/24
In Commercial Distribution

  • 10630094194117 ()
  • 00630094194110 ()


  • General-purpose surgical sponge

Abutment replica - 09321502016230

Laboratory component for prior generation Vistafix
Cochlear Bone Anchored Solutions AB
90374
In Commercial Distribution

  • 09321502016230 ()
90374

  • General external orthopaedic fixation system implantation kit, single-use

Guide pin 20 mm - 09321502016018

Laboratory component for prior generation Vistafix
Cochlear Bone Anchored Solutions AB
90796
In Commercial Distribution

  • 09321502016018 ()

  • 20 mm long guide pin
  • Length: 20 Millimeter
90796

  • General external orthopaedic fixation system implantation kit, single-use
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