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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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Moxi E Beige
Unitron Hearing Ltd
050-5578-01
In Commercial Distribution

  • 00698764443616 ()
050-5578-01

  • Air-conduction hearing aid, receiver-in-canal
Moxi2 E (beige)
Unitron Hearing Ltd
050-5622-01
In Commercial Distribution

  • 00698764504560 ()
050-5622-01

  • Air-conduction hearing aid, receiver-in-canal
Moxi2 E (cocoa)
Unitron Hearing Ltd
050-5622-E2
In Commercial Distribution

  • 00698764509701 ()
050-5622-E2

  • Air-conduction hearing aid, receiver-in-canal
Moxi2 E (champagne)
Unitron Hearing Ltd
050-5622-E1
In Commercial Distribution

  • 00698764509695 ()
050-5622-E1

  • Air-conduction hearing aid, receiver-in-canal
Moxi2 E (opal)
Unitron Hearing Ltd
050-5622-D8
In Commercial Distribution

  • 00698764509688 ()
050-5622-D8

  • Air-conduction hearing aid, receiver-in-canal
Moxi2 E (tungsten)
Unitron Hearing Ltd
050-5622-D7
In Commercial Distribution

  • 00698764509671 ()
050-5622-D7

  • Air-conduction hearing aid, receiver-in-canal
Moxi2 E (ivory)
Unitron Hearing Ltd
050-5622-D6
In Commercial Distribution

  • 00698764509664 ()
050-5622-D6

  • Air-conduction hearing aid, receiver-in-canal
Moxi2 E (stone)
Unitron Hearing Ltd
050-5622-D0
In Commercial Distribution

  • 00698764509640 ()
050-5622-D0

  • Air-conduction hearing aid, receiver-in-canal
M&E SPINE
MEDLINE INDUSTRIES, INC.
DYNJ909241
In Commercial Distribution

  • 10195327311124 ()
DYNJ909241

  • General surgical procedure kit, non-medicated, single-use
M&E SHOULDER
MEDLINE INDUSTRIES, INC.
DYNJ909239
In Commercial Distribution

  • 10195327311100 ()
DYNJ909239

  • General surgical procedure kit, non-medicated, single-use
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