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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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ZR7, KIT 312 2.4G NFM 90 R BE ZERENA 7
Bernafon AG
186012
In Commercial Distribution

  • 05711584084144 ()


  • Air-conduction hearing aid, in-the-ear
ZR7, KIT 312 2.4G NFM 85 PB R BE ZERENA 7
Bernafon AG
186008
In Commercial Distribution

  • 05711584084106 ()


  • Air-conduction hearing aid, in-the-ear
ZR7, KIT 312 2.4G NFM 85 L BE ZERENA 7
Bernafon AG
186007
In Commercial Distribution

  • 05711584084090 ()


  • Air-conduction hearing aid, in-the-ear
ZR7, KIT 312 2.4G NFM 85 R BE ZERENA 7
Bernafon AG
186006
In Commercial Distribution

  • 05711584084083 ()


  • Air-conduction hearing aid, in-the-ear
ZR7, KIT 312 2.4G NFM 75 L BE ZERENA 7
Bernafon AG
186005
In Commercial Distribution

  • 05711584084076 ()


  • Air-conduction hearing aid, in-the-ear
ZR7, KIT 312 2.4G NFM 75 R BE ZERENA 7
Bernafon AG
186004
In Commercial Distribution

  • 05711584084069 ()


  • Air-conduction hearing aid, in-the-ear
ZR9, KIT 312 NFM PB T L BE ZERENA 9
Bernafon AG
185934
In Commercial Distribution

  • 05711584084052 ()


  • Air-conduction hearing aid, in-the-ear
ZR9, KIT 312 NFM PB T R BE ZERENA 9
Bernafon AG
185933
In Commercial Distribution

  • 05711584084045 ()


  • Air-conduction hearing aid, in-the-ear
ZR9, KIT 312 NFM PB L BE ZERENA 9
Bernafon AG
185932
In Commercial Distribution

  • 05711584084038 ()


  • Air-conduction hearing aid, in-the-ear
ZR9, KIT 312 NFM PB R BE ZERENA 9
Bernafon AG
185931
In Commercial Distribution

  • 05711584084021 ()


  • Air-conduction hearing aid, in-the-ear
ZR9, KIT 312 NFM L BE ZERENA 9
Bernafon AG
185930
In Commercial Distribution

  • 05711584084014 ()


  • Air-conduction hearing aid, in-the-ear
ZR9, KIT 312 NFM R BE ZERENA 9
Bernafon AG
185929
In Commercial Distribution

  • 05711584084007 ()


  • Air-conduction hearing aid, in-the-ear
The VasoStat Hemostasis Device is used to augment hemostasis through a ratcheting pressure mechanism.
Forge Medical, Inc.
10348-325-04
In Commercial Distribution

  • 00863879000201 ()
  • 10863879000208 ()
  • 20863879000205 ()
  • 30863879000202 ()
  • 40863879000209 ()
  • 50863879000206 ()


  • Radial artery compression device
ZR9, KIT 312 NFM 90 PB R BE ZERENA 9
Bernafon AG
185927
In Commercial Distribution

  • 05711584083987 ()


  • Air-conduction hearing aid, in-the-ear
ZR9, KIT 312 NFM 90 R BE ZERENA 9
Bernafon AG
185925
In Commercial Distribution

  • 05711584083963 ()


  • Air-conduction hearing aid, in-the-ear
ZR9, KIT 312 NFM 85 PB T R BE ZERENA 9
Bernafon AG
185923
In Commercial Distribution

  • 05711584083949 ()


  • Air-conduction hearing aid, in-the-ear
ZR9, KIT 312 NFM 85 PB R BE ZERENA 9
Bernafon AG
185921
In Commercial Distribution

  • 05711584083925 ()


  • Air-conduction hearing aid, in-the-ear
NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed into bony voids or gaps of the skeletal system.
OSTEONOVUS, INC.
NGC05X
In Commercial Distribution

  • 00863787000461 ()

  • 5 cc


  • Bone matrix implant, synthetic, non-antimicrobial
ZR9, KIT 312 NFM 85 R BE ZERENA 9
Bernafon AG
185919
In Commercial Distribution

  • 05711584083901 ()


  • Air-conduction hearing aid, in-the-ear
NovoGro Putty is intended to be hydrated with ultra-pure water and gently packed into bony voids or gaps of the skeletal system.
OSTEONOVUS, INC.
NGC15
In Commercial Distribution

  • 00863787000430 ()


  • Bone matrix implant, synthetic, non-antimicrobial
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