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 - B504SRAR406890H0

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

  • B504SRAR406890H0 ()


  • Suturing unit, reprocessed

Arthrex - B504SRAR4068900

No Description
Provision
AR-4068-90
In Commercial Distribution

  • B504SRAR4068900 ()


  • Suturing unit, reprocessed

Arthrex - B504SRAR406845R0

No Description
Provision
AR-4068-45R
In Commercial Distribution

  • B504SRAR406845R0 ()


  • Suturing unit, reprocessed

Arthrex - B504SRAR406845L0

No Description
Provision
AR-4068-45L
In Commercial Distribution

  • B504SRAR406845L0 ()


  • Suturing unit, reprocessed

Arthrex - B504SRAR4068300

No Description
Provision
AR-4068-30
In Commercial Distribution

  • B504SRAR4068300 ()


  • Suturing unit, reprocessed

Arthrex - B504SRAR406825TR0

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

  • B504SRAR406825TR0 ()


  • Suturing unit, reprocessed

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
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