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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No Description
Provision
C7350
In Commercial Distribution

  • B504TCC73500 ()


  • Laparoscopic access cannula, reprocessed
No Description
Provision
C7344
In Commercial Distribution

  • B504TCC73440 ()


  • Laparoscopic access cannula, reprocessed
No Description
Provision
C7342
In Commercial Distribution

  • B504TCC73420 ()


  • Laparoscopic access cannula, reprocessed
No Description
Provision
C7334
In Commercial Distribution

  • B504TCC73340 ()


  • Laparoscopic access cannula, reprocessed
No Description
Provision
C7332
In Commercial Distribution

  • B504TCC73320 ()


  • Laparoscopic access cannula, reprocessed
No Description
Provision
C7324
In Commercial Distribution

  • B504TCC73240 ()


  • Laparoscopic access cannula, reprocessed
No Description
Provision
C7322
In Commercial Distribution

  • B504TCC73220 ()


  • Laparoscopic access cannula, reprocessed
No Description
Provision
C7312
In Commercial Distribution

  • B504TCC73120 ()


  • Laparoscopic access cannula, reprocessed
No Description
Provision
PEZS01A
In Commercial Distribution

  • B504TCPEZS01A0 ()


  • Laparoscopic access cannula, reprocessed
No Description
Provision
C7313
In Commercial Distribution

  • B504TCC73130 ()


  • Laparoscopic access cannula, reprocessed
No Description
Provision
9718
In Commercial Distribution

  • B504TC97180 ()


  • Laparoscopic access cannula, reprocessed
No Description
Provision
9704
In Commercial Distribution

  • B504TC97040 ()


  • Laparoscopic access cannula, reprocessed
No Description
Provision
C6387
In Commercial Distribution

  • B504SRC63870 ()


  • Suturing unit, reprocessed
No Description
Provision
C6386
In Commercial Distribution

  • B504SRC63860 ()


  • Suturing unit, reprocessed
No Description
Provision
C6385
In Commercial Distribution

  • B504SRC63850 ()


  • Suturing unit, reprocessed
No Description
Provision
C6384
In Commercial Distribution

  • B504SRC63840 ()


  • Suturing unit, reprocessed
No Description
Provision
C6383
In Commercial Distribution

  • B504SRC63830 ()


  • Suturing unit, reprocessed
No Description
Provision
C6382
In Commercial Distribution

  • B504SRC63820 ()


  • Suturing unit, reprocessed
No Description
Provision
C6381
In Commercial Distribution

  • B504SRC63810 ()


  • Suturing unit, reprocessed
No Description
Provision
C6380
In Commercial Distribution

  • B504SRC63800 ()


  • Suturing unit, reprocessed
No Description
Provision
C6362
In Commercial Distribution

  • B504SRC63620 ()


  • Suturing unit, reprocessed
No Description
Provision
C6112
In Commercial Distribution

  • B504SRC6112 ()


  • Drilling power tool attachment, basic
No Description
Provision
9599A
In Commercial Distribution

  • B504AS9599A0 ()


  • Arthroscopic shaver system blade, reprocessed
No Description
Provision
9399A
In Commercial Distribution

  • B504AS9399A0 ()


  • Arthroscopic shaver system blade, reprocessed
No Description
Provision
9392A
In Commercial Distribution

  • B504AS9392A0 ()


  • Arthroscopic shaver system blade, reprocessed
No Description
Provision
9391A
In Commercial Distribution

  • B504AS9391A0 ()


  • Arthroscopic shaver system blade, reprocessed
No Description
Provision
9299A
In Commercial Distribution

  • B504AS9299A0 ()


  • Arthroscopic shaver system blade, reprocessed
No Description
Provision
9298A
In Commercial Distribution

  • B504AS9298A0 ()


  • Arthroscopic shaver system blade, reprocessed
No Description
Provision
9297A
In Commercial Distribution

  • B504AS9297A0 ()


  • Arthroscopic shaver system blade, reprocessed
No Description
Provision
9247A
In Commercial Distribution

  • B504AS9247A0 ()


  • Arthroscopic shaver system blade, reprocessed
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