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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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scalpel blade fig 24 sterile p/100
Medicon eG. Chirurgiemechaniker-Genossenschaft
01.22.24
In Commercial Distribution

  • 04046826314415 ()
  • 04046826000110 ()
01.22.24

  • Manual scalpel blade, single-use
24 Deg Lordotic Trial, 20mm x 26mm
TITAN SPINE, LLC
7224-2520
Not in Commercial Distribution

  • 00191375042730 ()
7224-2520

  • Spinal implant trial
24 Deg Lordotic Trial, 19mm x 26mm
TITAN SPINE, LLC
7224-2519
Not in Commercial Distribution

  • 00191375042723 ()
7224-2519

  • Spinal implant trial
24 Deg Lordotic Trial, 18mm x 26mm
TITAN SPINE, LLC
7224-2518
Not in Commercial Distribution

  • 00191375042716 ()
7224-2518

  • Spinal implant trial
24 Deg Lordotic Trial, 17mm x 26mm
TITAN SPINE, LLC
7224-2517
Not in Commercial Distribution

  • 00191375042709 ()
7224-2517

  • Spinal implant trial
24 Deg Lordotic Trial, 16mm x 26mm
TITAN SPINE, LLC
7224-2516
Not in Commercial Distribution

  • 00191375042693 ()
7224-2516

  • Spinal implant trial
24 Deg Lordotic Trial, 20mm x 22mm
TITAN SPINE, LLC
7224-1520
Not in Commercial Distribution

  • 00191375042686 ()
7224-1520

  • Spinal implant trial
24 Deg Lordotic Trial, 19mm x 22mm
TITAN SPINE, LLC
7224-1519
Not in Commercial Distribution

  • 00191375042679 ()
7224-1519

  • Spinal implant trial
24 Deg Lordotic Trial, 18mm x 22mm
TITAN SPINE, LLC
7224-1518
Not in Commercial Distribution

  • 00191375042662 ()
7224-1518

  • Spinal implant trial
24 Deg Lordotic Trial, 17mm x 22mm
TITAN SPINE, LLC
7224-1517
Not in Commercial Distribution

  • 00191375042655 ()
7224-1517

  • Spinal implant trial
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