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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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No Description
Biomet Orthopedics, LLC
010002722
In Commercial Distribution

  • 00887868461842 ()

  • Size J
010002722

  • Orthopaedic implant impactor, reusable
No Description
Biomet Orthopedics, LLC
010002721
In Commercial Distribution

  • 00887868461835 ()

  • Size I
010002721

  • Orthopaedic implant impactor, reusable
No Description
Biomet Orthopedics, LLC
010002720
In Commercial Distribution

  • 00887868461828 ()

  • Size H
010002720

  • Orthopaedic implant impactor, reusable
No Description
Biomet Orthopedics, LLC
010002718
In Commercial Distribution

  • 00887868461804 ()

  • Size F
010002718

  • Orthopaedic implant impactor, reusable
No Description
Biomet Orthopedics, LLC
010002717
In Commercial Distribution

  • 00887868461798 ()

  • Size E
010002717

  • Orthopaedic implant impactor, reusable
No Description
Biomet Orthopedics, LLC
010002716
In Commercial Distribution

  • 00887868461781 ()

  • Size D
010002716

  • Orthopaedic implant impactor, reusable
No Description
Biomet Orthopedics, LLC
010002715
In Commercial Distribution

  • 00887868461774 ()

  • Size C
010002715

  • Orthopaedic implant impactor, reusable
No Description
Biomet Orthopedics, LLC
010002714
In Commercial Distribution

  • 00887868461767 ()

  • Size B
010002714

  • Orthopaedic implant impactor, reusable
No Description
Biomet Orthopedics, LLC
010002713
In Commercial Distribution

  • 00887868461750 ()

  • Size A
010002713

  • Orthopaedic implant impactor, reusable
Carton Assy, US, KAMRA Pod, Dispenser Carton Assembly
Bausch & Lomb Incorporated
76225-10
Not in Commercial Distribution

  • 00813359020052 ()
  • 00813359020069 ()


  • Corneal inlay, aperture reducing
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