SEARCH RESULTS FOR: gs1(42048 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 Class Implantable

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ACP - 00195377052865

ACP Drill, 23mm
Nuvasive, Inc.
7786763
In Commercial Distribution

  • 00195377052865 ()


  • Internal spinal fixation procedure kit, single-use

ACP - 00195377052858

ACP Drill, 22mm
Nuvasive, Inc.
7786762
In Commercial Distribution

  • 00195377052858 ()


  • Internal spinal fixation procedure kit, single-use

ACP - 00195377052841

ACP Drill, 21mm
Nuvasive, Inc.
7786761
In Commercial Distribution

  • 00195377052841 ()


  • Internal spinal fixation procedure kit, single-use

ACP - 00195377052834

ACP Drill, 20mm
Nuvasive, Inc.
7786760
In Commercial Distribution

  • 00195377052834 ()


  • Internal spinal fixation procedure kit, single-use

ACP - 00195377052827

ACP Drill, 19mm
Nuvasive, Inc.
7786759
In Commercial Distribution

  • 00195377052827 ()


  • Internal spinal fixation procedure kit, single-use

ACP - 00195377052810

ACP Drill, 18mm
Nuvasive, Inc.
7786758
In Commercial Distribution

  • 00195377052810 ()


  • Internal spinal fixation procedure kit, single-use

ACP - 00195377052803

ACP Drill, 17mm
Nuvasive, Inc.
7786757
In Commercial Distribution

  • 00195377052803 ()


  • Internal spinal fixation procedure kit, single-use

PULSE - 00195377052452

PULSE Slap Hammer
Nuvasive, Inc.
5050305
In Commercial Distribution

  • 00195377052452 ()


  • Orthopaedic stereotactic surgery system

PULSE - 00195377052445

PULSE Pin Cap
Nuvasive, Inc.
5050302
In Commercial Distribution

  • 00195377052445 ()


  • Orthopaedic stereotactic surgery system

PULSE - 00195377052438

PULSE Driver, Hexalobe
Nuvasive, Inc.
5050301
In Commercial Distribution

  • 00195377052438 ()


  • Orthopaedic stereotactic surgery system
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