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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40151602 Digital MDM, 30% Middle East
PARKER-HANNIFIN CORPORATION
91525265
In Commercial Distribution

  • 00816711023920 ()
91525265

  • Oxygen/air/nitrous oxide breathing gas mixer
40151615 Digital MDM, 30% Australia / N.Z.
PARKER-HANNIFIN CORPORATION
91525184
In Commercial Distribution

  • 00816711023876 ()
91525184

  • Oxygen/air/nitrous oxide breathing gas mixer
EAR GEL,VENT,WOE,MDM,BOX,6PCS
Gn Hearing A/S
22500400
In Commercial Distribution

  • 05708296260782 ()


  • Air-conduction hearing aid, in-the-ear
DOME,SF,OPEN,MDM,BAG,10 PCS
Gn Hearing A/S
19398300
In Commercial Distribution

  • 05708296067381 ()


  • Earmould, preformed
DOME,SF,PWR,MDM,BLSTR,8 PCS
Gn Hearing A/S
19399400
In Commercial Distribution

  • 05708296068999 ()


  • Earmould, preformed
DOME,SF,OPEN,MDM,BLSTR,8 PCS
Gn Hearing A/S
19399000
In Commercial Distribution

  • 05708296068951 ()


  • Earmould, preformed
DOME,THNTUB/REC,PWR,MDM,BAG,5
Gn Hearing A/S
18647300
In Commercial Distribution

  • 05708296068913 ()


  • Earmould, preformed
DOME,THNTUB/REC,SZ7,MDM,BAG,5
Gn Hearing A/S
18646900
In Commercial Distribution

  • 05708296068883 ()


  • Earmould, preformed
DOME,THNTUB/REC,SZ7,MDM,BAG,10
Gn Hearing A/S
18500900
In Commercial Distribution

  • 05708296067190 ()


  • Earmould, preformed
DOME,THNTUB/REC,PWR,MDM,BAG,10
Gn Hearing A/S
18265200
In Commercial Distribution

  • 05708296067176 ()


  • Earmould, preformed
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