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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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PULSE - 00195377051707

PULSE Cios Array Right
Nuvasive, Inc.
5050187
In Commercial Distribution

  • 00195377051707 ()


  • Orthopaedic stereotactic surgery system

PULSE - 00195377051547

PULSE Hip Pin Kit, 15cm
Nuvasive, Inc.
5050315
In Commercial Distribution

  • 00195377051547 ()


  • Orthopaedic stereotactic surgery system

PULSE - 00195377051530

PULSE Hip Pin Kit, 10cm
Nuvasive, Inc.
5050310
In Commercial Distribution

  • 00195377051530 ()


  • Orthopaedic stereotactic surgery system

PULSE - 00195377051523

PULSE AO Drill Bit, 4.0mm
Nuvasive, Inc.
5050273
In Commercial Distribution

  • 00195377051523 ()


  • Orthopaedic stereotactic surgery system

PULSE - 00195377051516

PULSE AO Drill Bit, 3.0mm
Nuvasive, Inc.
5050272
In Commercial Distribution

  • 00195377051516 ()


  • Orthopaedic stereotactic surgery system

PULSE - 00195377051509

PULSE 1/4 Square Drill Bit, 4.0mm
Nuvasive, Inc.
5050271
In Commercial Distribution

  • 00195377051509 ()


  • Orthopaedic stereotactic surgery system

PULSE - 00195377051011

PULSE Dual Patient Reference Array Kit
Nuvasive, Inc.
5050402
In Commercial Distribution

  • 00195377051011 ()


  • Orthopaedic stereotactic surgery system

PULSE - 00195377051004

PULSE Single Patient Reference Array Kit
Nuvasive, Inc.
5050401
In Commercial Distribution

  • 00195377051004 ()


  • Spinal rod bending system

PULSE - 00195377050298

PULSE 1/4 Square Drill Bit, 3.0mm
Nuvasive, Inc.
5050270
In Commercial Distribution

  • 00195377050298 ()


  • Orthopaedic stereotactic surgery system

PULSE - 00195377050281

PULSE Insulator, Drill Guide
Nuvasive, Inc.
5050269
In Commercial Distribution

  • 00195377050281 ()


  • Orthopaedic stereotactic surgery system
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