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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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SunMed - 20889483000547

CC BERMAN AIRWAYS 50mm BX/50
SUNMED, LLC
1-1506-50
In Commercial Distribution

  • 20889483000547 ()

  • Length: 5 Centimeter
1-1506-50

  • Oropharyngeal airway, single-use

SunMed - 20889483000530

CC BERMAN AIRWAYS 40mm BX/50
SUNMED, LLC
1-1506-40
In Commercial Distribution

  • 20889483000530 ()

  • Length: 4 Centimeter
1-1506-40

  • Oropharyngeal airway, single-use

SunMed - 20889483000523

CC BERMAN AIRWAYS 110mm BX/50
SUNMED, LLC
1-1506-11
In Commercial Distribution

  • 20889483000523 ()

  • Length: 11 Centimeter
1-1506-11

  • Oropharyngeal airway, single-use

MaXcess - 00887517093141

MAS TLIF C-C BLADE, LEFT 90mm
Nuvasive, Inc.
1542815
In Commercial Distribution

  • 00887517093141 ()


  • Surgical retraction system, reusable

MaXcess - 00887517093134

MAS TLIF C-C BLADE, LEFT 80mm
Nuvasive, Inc.
1542814
In Commercial Distribution

  • 00887517093134 ()


  • Surgical retraction system, reusable

MaXcess - 00887517093127

MAS TLIF C-C BLADE, LEFT 70mm
Nuvasive, Inc.
1542813
In Commercial Distribution

  • 00887517093127 ()


  • Surgical retraction system, reusable

MaXcess - 00887517093110

MAS TLIF C-C BLADE, LEFT 60mm
Nuvasive, Inc.
1542812
In Commercial Distribution

  • 00887517093110 ()


  • Surgical retraction system, reusable

MaXcess - 00887517093103

MAS TLIF C-C BLADE, LEFT 50mm
Nuvasive, Inc.
1542811
In Commercial Distribution

  • 00887517093103 ()


  • Surgical retraction system, reusable

MaXcess - 00887517092694

MAS TLIF C-C BLADE, RIGHT 90mm
Nuvasive, Inc.
1542805
In Commercial Distribution

  • 00887517092694 ()


  • Surgical retraction system, reusable

MaXcess - 00887517092687

MAS TLIF C-C BLADE, RIGHT 80mm
Nuvasive, Inc.
1542804
In Commercial Distribution

  • 00887517092687 ()


  • Surgical retraction system, reusable
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