SEARCH RESULTS FOR: arthrex*(7832 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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Arthrex - B504ASAR6420DS0

No Description
Provision
AR-6420DS
In Commercial Distribution

  • B504ASAR6420DS0 ()


  • Arthroscopic shaver system blade, reprocessed

Arthrex - B504ASAR6420BC0

No Description
Provision
AR-6420BC
In Commercial Distribution

  • B504ASAR6420BC0 ()


  • Arthroscopic shaver system blade, reprocessed

Arthrex - B504ARAS6420EX0

No Description
Provision
AR-6420EX
In Commercial Distribution

  • B504ARAS6420EX0 ()


  • Arthroscopic shaver system blade, reprocessed

Arthrex - B504AR87040

No Description
Provision
AR-8704
In Commercial Distribution

  • B504AR87041 ()
  • B504AR87040 ()


  • Suturing unit, reprocessed

Arthrex - B504AR87030

No Description
Provision
AR-8703
In Commercial Distribution

  • B504AR87031 ()
  • B504AR87030 ()


  • Suturing unit, reprocessed

Arthrex - B504AR87020

No Description
Provision
AR-8702
In Commercial Distribution

  • B504AR87021 ()
  • B504AR87020 ()


  • Suturing unit, reprocessed

Arthrex - B504AR87010

No Description
Provision
AR-8701
In Commercial Distribution

  • B504AR87011 ()
  • B504AR87010 ()


  • Suturing unit, reprocessed

Arthrex - B504AR4068CH0

No Description
Provision
AR-4068CH
In Commercial Distribution

  • B504AR4068CH0 ()


  • Suturing unit, reprocessed

Arthrex - B504AR4068C0

No Description
Provision
AR-4068C
In Commercial Distribution

  • B504AR4068C0 ()


  • Suturing unit, reprocessed

Arthrex - B504AR406890R0

No Description
Provision
AR-4068-90R
In Commercial Distribution

  • B504AR406890R0 ()


  • Suturing unit, reprocessed
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