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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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Sagittal/Coronal Head Bender, Left
Seaspine Orthopedics Corporation
91-6127
In Commercial Distribution

  • 10889981082390 ()
91-6127

  • Manual orthopaedic bender, reusable
Sagittal/Coronal Head Bender, Right
Seaspine Orthopedics Corporation
91-6126
In Commercial Distribution

  • 10889981082383 ()
91-6126

  • Manual orthopaedic bender, reusable
Angled In-Situ Bender 6.35mm, Left
Seaspine Orthopedics Corporation
91-6123
In Commercial Distribution

  • 10889981082352 ()

  • 6.35mm
91-6123

  • Manual orthopaedic bender, reusable
Angled In-Situ Bender, 6.35mm, Right
Seaspine Orthopedics Corporation
91-6122
In Commercial Distribution

  • 10889981082345 ()

  • 6.35mm
91-6122

  • Manual orthopaedic bender, reusable
Angled In-Situ Bender, Left
Seaspine Orthopedics Corporation
91-6121
In Commercial Distribution

  • 10889981082338 ()
91-6121

  • Manual orthopaedic bender, reusable
Angled In-Situ Bender, Right
Seaspine Orthopedics Corporation
91-6120
In Commercial Distribution

  • 10889981082321 ()
91-6120

  • Manual orthopaedic bender, reusable
French Rod Bender
Seaspine Orthopedics Corporation
91-2905
In Commercial Distribution

  • 10889981081973 ()
91-2905

  • Manual orthopaedic bender, reusable
FRENCH ROD BENDER
Seaspine Orthopedics Corporation
91-0907
In Commercial Distribution

  • 10889981080143 ()
91-0907

  • Manual orthopaedic bender, reusable
In-Situ Rod Bender, Right
Seaspine Orthopedics Corporation
91-0108
In Commercial Distribution

  • 10889981079567 ()
91-0108

  • Manual orthopaedic bender, reusable
In-Situ Rod Bender, Left
Seaspine Orthopedics Corporation
91-0107
In Commercial Distribution

  • 10889981079550 ()
91-0107

  • Manual orthopaedic bender, reusable
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