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 Segment,Size 4
WALDEMAR LINK GmbH & Co. KG
15-2978/02
In Commercial Distribution

  • 04026575328086 ()
15-2978/02

  • Knee arthroplasty wedge
Femoral Segment,Size 4
WALDEMAR LINK GmbH & Co. KG
15-2978/01
In Commercial Distribution

  • 04026575328079 ()
15-2978/01

  • Knee arthroplasty wedge
Femoral Segment,Size 4
WALDEMAR LINK GmbH & Co. KG
15-2977/02
In Commercial Distribution

  • 04026575328062 ()
15-2977/02

  • Knee arthroplasty wedge
Femoral Segment,Size 4
WALDEMAR LINK GmbH & Co. KG
15-2977/01
In Commercial Distribution

  • 04026575328055 ()
15-2977/01

  • Knee arthroplasty wedge
Femoral Segment,Size 4
WALDEMAR LINK GmbH & Co. KG
15-2964/05
In Commercial Distribution

  • 04026575205905 ()
15-2964/05

  • Knee arthroplasty wedge
Replacement Screw Femoral Augments
WALDEMAR LINK GmbH & Co. KG
ET18221
Not in Commercial Distribution

  • 04026575448647 ()
ET18221

  • Knee arthroplasty wedge
MK femoral spacer posterior
implantcast GmbH
5722601000
In Commercial Distribution

  • 04048844589554 ()

  • sz. 6 / 10 mm


  • Knee arthroplasty wedge
MK femoral spacer posterior
implantcast GmbH
5722501000
In Commercial Distribution

  • 04048844589547 ()

  • sz. 5 / 10 mm


  • Knee arthroplasty wedge
MK femoral spacer posterior
implantcast GmbH
5722401000
In Commercial Distribution

  • 04048844589530 ()

  • sz. 4 / 10 mm


  • Knee arthroplasty wedge
MK femoral spacer posterior
implantcast GmbH
5722301000
In Commercial Distribution

  • 04048844589523 ()

  • sz. 3 / 10 mm


  • Knee arthroplasty wedge
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