SEARCH RESULTS FOR: ("源头企业签名[Contact Telegram: duo785].hfs")(4912 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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GMK Sphere Revision Posterior Wedge S7 8mm
Medacta International SA
02.19.PE08
In Commercial Distribution

  • 07630345719034 ()


  • Knee arthroplasty wedge
GMK Sphere Revision Posterior Wedge S7 4mm
Medacta International SA
02.19.PE04
In Commercial Distribution

  • 07630345719027 ()


  • Knee arthroplasty wedge
GMK Sphere Revision Posterior Wedge S6 12mm
Medacta International SA
02.19.PD12
In Commercial Distribution

  • 07630345719010 ()


  • Knee arthroplasty wedge
GMK Sphere Revision Posterior Wedge S6 8mm
Medacta International SA
02.19.PD08
In Commercial Distribution

  • 07630345719003 ()


  • Knee arthroplasty wedge
GMK Sphere Revision Posterior Wedge S6 4mm
Medacta International SA
02.19.PD04
In Commercial Distribution

  • 07630345718990 ()


  • Knee arthroplasty wedge
GMK Sphere Revision Posterior Wedge S5 12mm
Medacta International SA
02.19.PC12
In Commercial Distribution

  • 07630345718983 ()


  • Knee arthroplasty wedge
GMK Sphere Revision Posterior Wedge S5 8mm
Medacta International SA
02.19.PC08
In Commercial Distribution

  • 07630345718976 ()


  • Knee arthroplasty wedge
GMK Sphere Revision Posterior Wedge S5 4mm
Medacta International SA
02.19.PC04
In Commercial Distribution

  • 07630345718969 ()


  • Knee arthroplasty wedge
GMK Sphere Revision Posterior Wedge S3/4 12mm
Medacta International SA
02.19.PB12
In Commercial Distribution

  • 07630345718952 ()


  • Knee arthroplasty wedge
GMK Sphere Revision Posterior Wedge S3/4 8mm
Medacta International SA
02.19.PB08
In Commercial Distribution

  • 07630345718945 ()


  • Knee arthroplasty wedge
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