SEARCH RESULTS FOR: 安信11平台链接【球球4120051】✅.krg(40468 results)

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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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Tibial Augment
WALDEMAR LINK GmbH & Co. KG
880-335/11
In Commercial Distribution

  • 04026575258321 ()
880-335/11

  • Knee arthroplasty wedge
Tibial Augment
WALDEMAR LINK GmbH & Co. KG
880-333/11
In Commercial Distribution

  • 04026575258260 ()
880-333/11

  • Knee arthroplasty wedge
Tibial Augment
WALDEMAR LINK GmbH & Co. KG
880-331/11
In Commercial Distribution

  • 04026575258192 ()
880-331/11

  • Knee arthroplasty wedge
Femoral Augment, Posterior
WALDEMAR LINK GmbH & Co. KG
880-319/11
In Commercial Distribution

  • 04026575257942 ()
880-319/11

  • Knee arthroplasty wedge
Femoral Augment, Posterior
WALDEMAR LINK GmbH & Co. KG
880-317/11
In Commercial Distribution

  • 04026575257843 ()
880-317/11

  • Knee arthroplasty wedge
Femoral Augment, Posterior
WALDEMAR LINK GmbH & Co. KG
880-315/11
In Commercial Distribution

  • 04026575257768 ()
880-315/11

  • Knee arthroplasty wedge
Femoral Augment, Posterior
WALDEMAR LINK GmbH & Co. KG
880-313/11
In Commercial Distribution

  • 04026575257621 ()
880-313/11

  • Knee arthroplasty wedge
Femoral Augment, Posterior
WALDEMAR LINK GmbH & Co. KG
880-311/11
In Commercial Distribution

  • 04026575257607 ()
880-311/11

  • Knee arthroplasty wedge
Femoral Augment, Posterior
WALDEMAR LINK GmbH & Co. KG
880-310/11
In Commercial Distribution

  • 04026575257539 ()
880-310/11

  • Knee arthroplasty wedge
Femoral Augment, Distal
WALDEMAR LINK GmbH & Co. KG
880-309/11
In Commercial Distribution

  • 04026575257454 ()
880-309/11

  • Knee arthroplasty wedge
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