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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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Femoral Component, CR
WALDEMAR LINK GmbH & Co. KG
880-010/40
In Commercial Distribution

  • 04026575247080 ()
880-010/40

  • Uncoated knee femur prosthesis, metallic
Femoral Component, CR
WALDEMAR LINK GmbH & Co. KG
880-010/35
In Commercial Distribution

  • 04026575247073 ()
880-010/35

  • Uncoated knee femur prosthesis, metallic
Femoral Component, CR
WALDEMAR LINK GmbH & Co. KG
880-010/30
In Commercial Distribution

  • 04026575247066 ()
880-010/30

  • Uncoated knee femur prosthesis, metallic
Articulating Surfaces, PS
WALDEMAR LINK GmbH & Co. KG
880-251/10
In Commercial Distribution

  • 04026575246298 ()
880-251/10

  • Uncoated knee tibia prosthesis, polyethylene
Articulating Surfaces, CR
WALDEMAR LINK GmbH & Co. KG
880-241/10
In Commercial Distribution

  • 04026575246281 ()
880-241/10

  • Uncoated knee tibia prosthesis, polyethylene
Articulating Surfaces, CCK
WALDEMAR LINK GmbH & Co. KG
880-231/10
In Commercial Distribution

  • 04026575245475 ()
880-231/10

  • Uncoated knee tibia prosthesis, polyethylene
Articulating Surfaces, PS+
WALDEMAR LINK GmbH & Co. KG
880-221/10
In Commercial Distribution

  • 04026575245314 ()
880-221/10

  • Uncoated knee tibia prosthesis, polyethylene
Articulating Surfaces, PS
WALDEMAR LINK GmbH & Co. KG
880-211/12
In Commercial Distribution

  • 04026575245307 ()
880-211/12

  • Uncoated knee tibia prosthesis, polyethylene
Articulating Surfaces, CR
WALDEMAR LINK GmbH & Co. KG
880-201/10
In Commercial Distribution

  • 04026575245291 ()
880-201/10

  • Uncoated knee tibia prosthesis, polyethylene
Tibial Component, Modular
WALDEMAR LINK GmbH & Co. KG
880-100/10
In Commercial Distribution

  • 04026575245239 ()
880-100/10

  • Coated knee tibia prosthesis
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