SEARCH RESULTS FOR: gs1(4853 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 Class Implantable

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ReLine - 00887517045034

RELINE MAS Kwireless Stylet, 50mm Long
Nuvasive, Inc.
1778558P
In Commercial Distribution

  • 00887517045034 ()


  • Internal spinal fixation procedure kit, single-use

ReLine - 00887517045027

RELINE MAS Kwireless Stylet, 45mm Long
Nuvasive, Inc.
1778557P
In Commercial Distribution

  • 00887517045027 ()


  • Internal spinal fixation procedure kit, single-use

ReLine - 00887517045010

RELINE MAS Kwireless Stylet, 40mm Long
Nuvasive, Inc.
1778556P
In Commercial Distribution

  • 00887517045010 ()


  • Internal spinal fixation procedure kit, single-use

ReLine - 00887517045003

RELINE MAS Kwireless Stylet, 35mm Long
Nuvasive, Inc.
1778555P
In Commercial Distribution

  • 00887517045003 ()


  • Internal spinal fixation procedure kit, single-use

ReLine - 00887517044990

RELINE MAS Kwireless Stylet, 55mm
Nuvasive, Inc.
1001820
In Commercial Distribution

  • 00887517044990 ()


  • Internal spinal fixation procedure kit, single-use

ReLine - 00887517044983

RELINE MAS Kwireless Stylet, 50mm
Nuvasive, Inc.
1001815
In Commercial Distribution

  • 00887517044983 ()


  • Internal spinal fixation procedure kit, single-use

ReLine - 00887517044976

RELINE MAS Kwireless Stylet, 45mm
Nuvasive, Inc.
1001813
In Commercial Distribution

  • 00887517044976 ()


  • Internal spinal fixation procedure kit, single-use

ReLine - 00887517044969

RELINE MAS Kwireless Stylet, 40mm
Nuvasive, Inc.
1001805
In Commercial Distribution

  • 00887517044969 ()


  • Internal spinal fixation procedure kit, single-use

ReLine - 00887517044952

RELINE MAS Kwireless Stylet, 35mm
Nuvasive, Inc.
1001804
In Commercial Distribution

  • 00887517044952 ()


  • Internal spinal fixation procedure kit, single-use

NuVasive - 00887517533982

Universal Threaded Pin, Bone Mill
Nuvasive, Inc.
1690388
In Commercial Distribution

  • 00887517533982 ()


  • Bone distraction forceps
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