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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
880-333/13
In Commercial Distribution

  • 04026575258284 ()
880-333/13

  • 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
880-331/22
In Commercial Distribution

  • 04026575258246 ()
880-331/22

  • Knee arthroplasty wedge
Tibial Augment
WALDEMAR LINK GmbH & Co. KG
880-331/21
In Commercial Distribution

  • 04026575258222 ()
880-331/21

  • 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, L-Shaped
WALDEMAR LINK GmbH & Co. KG
880-329/23
In Commercial Distribution

  • 04026575258185 ()
880-329/23

  • Knee arthroplasty wedge
Femoral Augment, L-Shaped
WALDEMAR LINK GmbH & Co. KG
880-327/23
In Commercial Distribution

  • 04026575258161 ()
880-327/23

  • Knee arthroplasty wedge
Femoral Augment, L-Shaped
WALDEMAR LINK GmbH & Co. KG
880-325/13
In Commercial Distribution

  • 04026575258123 ()
880-325/13

  • Knee arthroplasty wedge
Femoral Augment, L-Shaped
WALDEMAR LINK GmbH & Co. KG
880-321/22
In Commercial Distribution

  • 04026575258079 ()
880-321/22

  • Knee arthroplasty wedge
Femoral Augment, Posterior
WALDEMAR LINK GmbH & Co. KG
880-319/22
In Commercial Distribution

  • 04026575257973 ()
880-319/22

  • Knee arthroplasty wedge
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