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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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E-Pack Procedure Kit
Ethicon Inc.
9808E
Not in Commercial Distribution

  • 30705031241835 ()
  • 20705031241838 ()
9808E

  • General surgical procedure kit, non-medicated, single-use
E-Pack Procedure Kit
Ethicon Inc.
9871E
Not in Commercial Distribution

  • 30705031241712 ()
  • 20705031241715 ()
9871E

  • General surgical procedure kit, non-medicated, single-use
E-Pack Procedure Kit
Ethicon Inc.
9896E
Not in Commercial Distribution

  • 30705031241699 ()
  • 20705031241692 ()
9896E

  • General surgical procedure kit, non-medicated, single-use
E-Pack Procedure Kit
Ethicon Inc.
9875E
Not in Commercial Distribution

  • 30705031241668 ()
  • 20705031241661 ()
9875E

  • General surgical procedure kit, non-medicated, single-use
E-Pack Procedure Kit
Ethicon Inc.
9885E
Not in Commercial Distribution

  • 30705031241620 ()
  • 20705031241623 ()
9885E

  • General surgical procedure kit, non-medicated, single-use
E-Pack Procedure Kit
Ethicon Inc.
9892E
Not in Commercial Distribution

  • 30705031241576 ()
  • 20705031241579 ()
9892E

  • General surgical procedure kit, non-medicated, single-use
E-Pack Procedure Kit
Ethicon Inc.
9891E
Not in Commercial Distribution

  • 30705031241507 ()
  • 20705031241500 ()
9891E

  • General surgical procedure kit, non-medicated, single-use
Circular Mapping Catheter
Biosense Webster Inc
D140403
In Commercial Distribution

  • 10846835020359 ()
D140403

  • Cardiac mapping catheter, percutaneous, single-use
Circular Mapping Catheter
Biosense Webster Inc
D140402
In Commercial Distribution

  • 10846835020342 ()
D140402

  • Cardiac mapping catheter, percutaneous, single-use
Circular Mapping Catheter
Biosense Webster Inc
D140401
In Commercial Distribution

  • 10846835020335 ()
D140401

  • Cardiac mapping catheter, percutaneous, single-use
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