SEARCH RESULTS FOR: (*d47 external mil*)(510271 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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MEDI - 00636257014134

!20-30 SHRINKER AK 12" LONG BLACK SZ 3
MEDI MANUFACTURING, INC.
KAK1L5W3
In Commercial Distribution

  • 00636257014134 ()


  • Limb-worn device hygienic cover

MEDI - 00636257014127

!20-30 SHRINKER AK 12" LONG BLACK SZ 2
MEDI MANUFACTURING, INC.
KAK1L5W2
In Commercial Distribution

  • 00636257014127 ()


  • Limb-worn device hygienic cover

MEDI - 00636257014110

!20-30 SHRINKER AK 12" LONG BLACK SZ 1
MEDI MANUFACTURING, INC.
KAK1L5W1
In Commercial Distribution

  • 00636257014110 ()


  • Limb-worn device hygienic cover

MEDI - 00636257014103

!20-30 SHRINKER AK 12" LONG BEIGE SZ 6
MEDI MANUFACTURING, INC.
KAK1L0W6
In Commercial Distribution

  • 00636257014103 ()


  • Limb-worn device hygienic cover

MEDI - 00636257014097

!20-30 SHRINKER AK 12" LONG BEIGE SZ 5
MEDI MANUFACTURING, INC.
KAK1L0W5
In Commercial Distribution

  • 00636257014097 ()


  • Limb-worn device hygienic cover

MEDI - 00636257014080

!20-30 SHRINKER AK 12" LONG BEIGE SZ 4
MEDI MANUFACTURING, INC.
KAK1L0W4
In Commercial Distribution

  • 00636257014080 ()


  • Limb-worn device hygienic cover

MEDI - 00636257014073

!20-30 SHRINKER AK 12" LONG BEIGE SZ 3
MEDI MANUFACTURING, INC.
KAK1L0W3
In Commercial Distribution

  • 00636257014073 ()


  • Limb-worn device hygienic cover

MEDI - 00636257014066

!20-30 SHRINKER AK 12" LONG BEIGE SZ 2
MEDI MANUFACTURING, INC.
KAK1L0W2
In Commercial Distribution

  • 00636257014066 ()


  • Limb-worn device hygienic cover

MEDI - 00636257014059

!20-30 SHRINKER AK 12" LONG BEIGE SZ 1
MEDI MANUFACTURING, INC.
KAK1L0W1
In Commercial Distribution

  • 00636257014059 ()


  • Limb-worn device hygienic cover

RehaStim 2 - 04260397620670

External Functional Neuromuscular Stimulator (8 channels), designed for use as stand-alone device as well as in combination with exercise equipment for walking and cycling applications, that has been validated for compatibility by HASOMED GmbH and should be used under the supervision of a clinician. - manufactured for use in system
HASOMED GmbH
FES01050
In Commercial Distribution

  • 04260397620670 ()
FES01050

  • Gait-enhancement electrical stimulation system, external
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