SEARCH RESULTS FOR: arthrex*(7828 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 - B504SRAR406825TL0

No Description
Provision
AR-4068-25TL
In Commercial Distribution

  • B504SRAR406825TL0 ()


  • Suturing unit, reprocessed

Arthrex - B504SRAR4065W0

No Description
Provision
AR-4065W
In Commercial Distribution

  • B504SRAR4065W0 ()


  • Suturing unit, reprocessed

Arthrex - B504SRAR4065S0

No Description
Provision
AR-4065S
In Commercial Distribution

  • B504SRAR4065S0 ()


  • Suturing unit, reprocessed

Arthrex - B504SRAR4065B0

No Description
Provision
AR-4065B
In Commercial Distribution

  • B504SRAR4065B0 ()


  • Suturing unit, reprocessed

Arthrex - B504SRAR406590W0

No Description
Provision
AR-4065-90W
In Commercial Distribution

  • B504SRAR406590W0 ()


  • Suturing unit, reprocessed

Arthrex - B504SRAR406590S0

No Description
Provision
AR-4065-90S
In Commercial Distribution

  • B504SRAR406590S0 ()


  • Suturing unit, reprocessed

Arthrex - B504SRAR406545R0

No Description
Provision
AR-4065-45R
In Commercial Distribution

  • B504SRAR406545R0 ()


  • Suturing unit, reprocessed

Arthrex - B504SRAR406545L0

No Description
Provision
AR-4065-45L
In Commercial Distribution

  • B504SRAR406545L0 ()


  • Suturing unit, reprocessed

Arthrex - B504SRAR16992N0

No Description
Provision
AR-16992N
In Commercial Distribution

  • B504SRAR16992N0 ()


  • Suturing unit, reprocessed

Arthrex - B504SRAR16991N0

No Description
Provision
AR-16991N
In Commercial Distribution

  • B504SRAR16991N0 ()


  • Suturing unit, reprocessed
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