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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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Bencox Mirabo PE Liner Trial 28C+-STD-PPX
Corentec Co., Ltd
HA.01K.2842
In Commercial Distribution

  • 08800068949455 ()


  • Surgical implant/trial-implant/sizer holder, reusable
Bencox Mirabo PE Liner Trial 28D-STD-PPX
Corentec Co., Ltd
HA.01K.2844
In Commercial Distribution

  • 08800068949448 ()


  • Surgical implant/trial-implant/sizer holder, reusable
Bencox Mirabo PE Liner Trial 28E-STD-PPX
Corentec Co., Ltd
HA.01K.2848
In Commercial Distribution

  • 08800068949431 ()


  • Surgical implant/trial-implant/sizer holder, reusable
Bencox Mirabo PE Liner Trial 28F-STD-PPX
Corentec Co., Ltd
HA.01K.2852
In Commercial Distribution

  • 08800068949424 ()


  • Surgical implant/trial-implant/sizer holder, reusable
Bencox Mirabo PE Liner Trial 32C-STD-PPX
Corentec Co., Ltd
HA.01K.3239
In Commercial Distribution

  • 08800068949417 ()


  • Surgical implant/trial-implant/sizer holder, reusable
Bencox Mirabo PE Liner Trial 32C+-STD-PPX
Corentec Co., Ltd
HA.01K.3242
In Commercial Distribution

  • 08800068949394 ()


  • Surgical implant/trial-implant/sizer holder, reusable
Bencox Mirabo PE Liner Trial 32D-STD-PPX
Corentec Co., Ltd
HA.01K.3244
In Commercial Distribution

  • 08800068949387 ()


  • Surgical implant/trial-implant/sizer holder, reusable
Bencox Mirabo PE Liner Trial 32E-STD-PPX
Corentec Co., Ltd
HA.01K.3248
In Commercial Distribution

  • 08800068949370 ()


  • Surgical implant/trial-implant/sizer holder, reusable
Bencox Mirabo PE Liner Trial 32F-STD-PPX
Corentec Co., Ltd
HA.01K.3252
In Commercial Distribution

  • 08800068949363 ()


  • Surgical implant/trial-implant/sizer holder, reusable
Bencox Mirabo PE Liner Trial 36C+-STD-PPX
Corentec Co., Ltd
HA.01K.3642
In Commercial Distribution

  • 08800068949356 ()


  • Surgical implant/trial-implant/sizer holder, reusable
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