SEARCH RESULTS FOR: ("源头企业签名[Contact Telegram: duo785].hfs")(12124 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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Screwed Tibial Augmentation # 1/20 mm (RM/LL)
Medacta International SA
02.09.TA120RMLL
In Commercial Distribution

  • 07630030876905 ()


  • Knee arthroplasty wedge
Screwed Tibial Augmentation # 1/20 mm (LM/RL)
Medacta International SA
02.09.TA120LMRL
In Commercial Distribution

  • 07630030876899 ()


  • Knee arthroplasty wedge
Screwed Tibial Augmentation # 1/15 mm (RM/LL)
Medacta International SA
02.09.TA115RMLL
In Commercial Distribution

  • 07630030876882 ()


  • Knee arthroplasty wedge
Screwed Tibial Augmentation # 1/15 mm (LM/RL)
Medacta International SA
02.09.TA115LMRL
In Commercial Distribution

  • 07630030876875 ()


  • Knee arthroplasty wedge
Femoral Augmentation distal # 3/16 mm
Medacta International SA
02.07.316FDA
In Commercial Distribution

  • 07630030888908 ()


  • Knee arthroplasty wedge
Femoral Augmentation distal # 2/20 mm
Medacta International SA
02.07.220FDA
In Commercial Distribution

  • 07630030888892 ()


  • Knee arthroplasty wedge
Femoral Augmentation distal # 2/16 mm
Medacta International SA
02.07.216FDA
In Commercial Distribution

  • 07630030888885 ()


  • Knee arthroplasty wedge
Femoral Augmentation distal # 1/20 mm
Medacta International SA
02.07.120FDA
In Commercial Distribution

  • 07630030888878 ()


  • Knee arthroplasty wedge
Femoral Augmentation distal # 1/16 mm
Medacta International SA
02.07.116FDA
In Commercial Distribution

  • 07630030888861 ()


  • Knee arthroplasty wedge
Femoral Augmentation distal # 6/12 mm
Medacta International SA
02.07.612FDA
In Commercial Distribution

  • 07630030885501 ()


  • Knee arthroplasty wedge
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