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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MICROMOVEMENT LOCKING NUT FOR PROCALLUS
ORTHOFIX SRL
1
In Commercial Distribution

  • 18032568861105 ()
90015

  • External orthopaedic fixation system, reusable
PROCALLUS CLAMP SCREW
ORTHOFIX SRL
1
In Commercial Distribution

  • 18032568861099 ()
90014

  • External orthopaedic fixation system, reusable
PROCALLUS T-CLAMP
ORTHOFIX SRL
1
In Commercial Distribution

  • 18032568861068 ()
90007

  • External orthopaedic fixation system, reusable
PROCALLUS STANDARD BODY
ORTHOFIX SRL
1
In Commercial Distribution

  • 18032568861020 ()
90002

  • External orthopaedic fixation system, reusable
RING LOCKING SCREW
ORTHOFIX SRL
1
In Commercial Distribution

  • 18032568860689 ()
81008

  • External orthopaedic fixation system, reusable
2/3 RING INNER DIAMETER 150MM
ORTHOFIX SRL
1
In Commercial Distribution

  • 18032568860603 ()

  • Width: 147 Millimeter
81000A

  • External orthopaedic fixation system, reusable
8/10 MM SPANNER
ORTHOFIX SRL
1
In Commercial Distribution

  • 18032568860511 ()

  • Width: 145 Millimeter
80075

  • External orthopaedic fixation system, reusable
ASSEMBLY KIT SHORT FOR HYBRID PROCALLUS
ORTHOFIX SRL
1
In Commercial Distribution

  • 18032568860474 ()
80052

  • External orthopaedic fixation system, reusable
ASSEMBLY KIT STANDARD FOR HYBRID PROCALLUS
ORTHOFIX SRL
1
In Commercial Distribution

  • 18032568860467 ()
80051

  • External orthopaedic fixation system, reusable
HYBRID COUPLING WITH BALL-JOINT
ORTHOFIX SRL
1
In Commercial Distribution

  • 18032568860450 ()
80050

  • External orthopaedic fixation system, reusable
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