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 - B504SRAR8690SLL0

No Description
Provision
AR-8690SLL
In Commercial Distribution

  • B504SRAR8690SLL0 ()


  • Suturing unit, reprocessed

Arthrex - B504SRAR4068CH0

No Description
Provision
AR-4068CH
In Commercial Distribution

  • B504SRAR4068CH0 ()


  • Suturing unit, reprocessed

Arthrex - B504SRAR4068C0

No Description
Provision
AR-4068C
In Commercial Distribution

  • B504SRAR4068C0 ()


  • Suturing unit, reprocessed

Arthrex - B504SRAR406890R0

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

  • B504SRAR406890R0 ()


  • Suturing unit, reprocessed

Arthrex - B504SRAR406890L0

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

  • B504SRAR406890L0 ()


  • Suturing unit, reprocessed

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
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