SEARCH RESULTS FOR: (*Fake Texas A*)(10489 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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ALTIUS™ M-INI™ OCT - 00880304975255

No Description
BIOMET SPINE LLC
1200-3010
In Commercial Distribution

  • 00880304975255 ()

  • ALTIUS OCCIPITAL BONE SCREW 5.0MM (D) X 10MM (L)
1200-3010

  • Bone-screw internal spinal fixation system, non-sterile

ALTIUS™ M-INI™ OCT - 00880304975248

No Description
BIOMET SPINE LLC
1200-3011
In Commercial Distribution

  • 00880304975248 ()

  • ALTIUS OCCIPITAL BONE SCREW 5.0MM (D) X 11MM (L)
1200-3011

  • Bone-screw internal spinal fixation system, non-sterile

ALTIUS™ M-INI™ OCT - 00880304975231

No Description
BIOMET SPINE LLC
1200-3012
In Commercial Distribution

  • 00880304975231 ()

  • ALTIUS OCCIPITAL BONE SCREW 5.0MM (D) X 12MM (L)
1200-3012

  • Bone-screw internal spinal fixation system, non-sterile

ALTIUS™ M-INI™ OCT - 00880304975224

No Description
BIOMET SPINE LLC
1200-3013
In Commercial Distribution

  • 00880304975224 ()

  • ALTIUS OCCIPITAL BONE SCREW 5.0MM (D) X 13MM (L)
1200-3013

  • Bone-screw internal spinal fixation system, non-sterile

ALTIUS™ M-INI™ OCT - 00880304975217

No Description
BIOMET SPINE LLC
1200-3014
In Commercial Distribution

  • 00880304975217 ()

  • ALTIUS OCCIPITAL BONE SCREW 5.0MM (D) X 14MM (L)
1200-3014

  • Bone-screw internal spinal fixation system, non-sterile

ALTIUS™ M-INI™ OCT - 00880304975200

No Description
BIOMET SPINE LLC
1200-3015
In Commercial Distribution

  • 00880304975200 ()

  • ALTIUS OCCIPITAL BONE SCREW 5.0MM (D) X 15MM (L)
1200-3015

  • Bone-screw internal spinal fixation system, non-sterile

ALTIUS™ M-INI™ OCT - 00880304975194

No Description
BIOMET SPINE LLC
1200-3016
In Commercial Distribution

  • 00880304975194 ()

  • ALTIUS OCCIPITAL BONE SCREW 5.0MM (D) X 16MM (L)
1200-3016

  • Bone-screw internal spinal fixation system, non-sterile

ALTIUS™ M-INI™ OCT - 00880304975187

No Description
BIOMET SPINE LLC
1200-3017
In Commercial Distribution

  • 00880304975187 ()

  • ALTIUS OCCIPITAL BONE SCREW 5.0MM (D) X 17MM (L)
1200-3017

  • Bone-screw internal spinal fixation system, non-sterile

ALTIUS™ M-INI™ OCT - 00880304975170

No Description
BIOMET SPINE LLC
1200-3018
In Commercial Distribution

  • 00880304975170 ()

  • ALTIUS OCCIPITAL BONE SCREW 5.0MM (D) X 18MM (L)
1200-3018

  • Bone-screw internal spinal fixation system, non-sterile

ALTIUS™ M-INI™ OCT - 00880304975163

No Description
BIOMET SPINE LLC
1200-3019
In Commercial Distribution

  • 00880304975163 ()

  • ALTIUS OCCIPITAL BONE SCREW 5.0MM (D) X 19MM (L)
1200-3019

  • Bone-screw internal spinal fixation system, non-sterile

ALTIUS™ M-INI™ OCT - 00880304975156

No Description
BIOMET SPINE LLC
1200-3020
In Commercial Distribution

  • 00880304975156 ()

  • ALTIUS OCCIPITAL BONE SCREW 5.0MM (D) X 20MM (L)
1200-3020

  • Bone-screw internal spinal fixation system, non-sterile

Merit Advance® - 00884450151839

No Description
Merit Medical Systems, Inc.
00884450151839
In Commercial Distribution

  • 10884450151836 ()
  • 00884450151839 ()
  • 20884450151833 ()

  • Accepts Guide Wire-0.021" (0.53 mm)
  • Length (cm)-9.0 cm
  • Gauge-21G


  • Vascular catheter introduction needle

Merit Advance® - 00884450151815

No Description
Merit Medical Systems, Inc.
00884450151815
In Commercial Distribution

  • 10884450151812 ()
  • 00884450151815 ()
  • 20884450151819 ()

  • Length (cm)-7.0 cm
  • Accepts Guide Wire-0.021" (0.53 mm)
  • Gauge-21G


  • Vascular catheter introduction needle

Merit Advance® - 00884450151792

No Description
Merit Medical Systems, Inc.
00884450151792
In Commercial Distribution

  • 20884450151796 ()
  • 10884450151799 ()
  • 00884450151792 ()

  • Gauge-21G
  • Accepts Guide Wire-0.021" (0.53 mm)
  • Length (cm)-7.0 cm


  • Basic intravenous administration set, noninvasive

Merit Advance® - 00884450151778

No Description
Merit Medical Systems, Inc.
00884450151778
In Commercial Distribution

  • 10884450151775 ()
  • 00884450151778 ()
  • 20884450151772 ()

  • Length (cm)-4.0 cm
  • Gauge-21G
  • Accepts Guide Wire-0.021" (0.53 mm)


  • Basic intravenous administration set, noninvasive

Merit Advance® - 00884450151754

No Description
Merit Medical Systems, Inc.
00884450151754
In Commercial Distribution

  • 10884450151751 ()
  • 00884450151754 ()
  • 20884450151758 ()

  • Length (cm)-4.0 cm
  • Gauge-21G
  • Accepts Guide Wire-0.021" (0.53 mm)


  • Basic intravenous administration set, noninvasive

LIFEPAK® 12 defibrillator/monitor - 00721902301278

LP12AABBBBBAABBAAAAAAAAALP12 MONITOR-DEFIB
PHYSIO-CONTROL, INC.
97400
Not in Commercial Distribution

  • 00721902301278 ()
97400-000185

  • Physiologic-monitoring defibrillation system

LIFEPAK® 500 Automated External Defibrillator - 00721902275883

LP500AACAAZZZZZLP500EECGIAAAAEAZZZZZ
PHYSIO-CONTROL, INC.
99401
Not in Commercial Distribution

  • 00721902275883 ()
99401-000524

  • Non-rechargeable public semi-automated external defibrillator

LIFEPAK® 12 defibrillator/monitor - 00721902206917

LP12AABBBBAABABAAABAAAAALP12 MONITOR-DEFIB
PHYSIO-CONTROL, INC.
99400
Not in Commercial Distribution

  • 00721902206917 ()
99400-001245

  • Physiologic-monitoring defibrillation system

LIFEPAK® 12 defibrillator/monitor - 00721902188077

LP12AABBBBBABABBAABAAAAALP12 MONITOR-DEFIB
PHYSIO-CONTROL, INC.
99400
Not in Commercial Distribution

  • 00721902188077 ()
99400-001229

  • Physiologic-monitoring defibrillation system

LIFEPAK® 12 defibrillator/monitor - 00721902180804

LP12AABABBBABBABAABAAAAALP12 MONITOR-DEFIB
PHYSIO-CONTROL, INC.
99400
Not in Commercial Distribution

  • 00721902180804 ()
99400-001206

  • Physiologic-monitoring defibrillation system

LIFEPAK® 500 Automated External Defibrillator - 00721902174377

LP500AACBBZZZZZLP500EECGIAAAAABZZZZZ
PHYSIO-CONTROL, INC.
99401
Not in Commercial Distribution

  • 00721902174377 ()
99401-000392

  • Non-rechargeable public semi-automated external defibrillator

LIFEPAK® 500 Automated External Defibrillator - 00721902174353

LP500AACABZZZZZLP500EECGIAAAABBZZZZZ
PHYSIO-CONTROL, INC.
99401
Not in Commercial Distribution

  • 00721902174353 ()
99401-000390

  • Non-rechargeable public semi-automated external defibrillator

LIFEPAK® 500 Automated External Defibrillator - 00721902174339

LP500AACAAZZZZZLP500EECGIAAAABAZZZZZ
PHYSIO-CONTROL, INC.
99401
Not in Commercial Distribution

  • 00721902174339 ()
99401-000388

  • Non-rechargeable public semi-automated external defibrillator

LIFEPAK® 12 defibrillator/monitor - 00721902154119

LP12AABBBBBABBABAABAAAAALP12 MONITOR-DEFIB
PHYSIO-CONTROL, INC.
99400
Not in Commercial Distribution

  • 00721902154119 ()
99400-000937

  • Physiologic-monitoring defibrillation system

LIFEPAK® 12 defibrillator/monitor - 00721902153846

LP12AABABBBABABBAAAAAAAALP12 MONITOR-DEFIB
PHYSIO-CONTROL, INC.
99400
Not in Commercial Distribution

  • 00721902153846 ()
99400-000910

  • Physiologic-monitoring defibrillation system

LIFEPAK® 12 defibrillator/monitor - 00721902153808

LP12AABBBBAABBBBAABAAAAALP12 MONITOR-DEFIB
PHYSIO-CONTROL, INC.
99400
Not in Commercial Distribution

  • 00721902153808 ()
99400-000906

  • Physiologic-monitoring defibrillation system

LIFEPAK® 12 defibrillator/monitor - 00721902152962

LP12AABBBBAABBBBBABAAAAALP12 MONITOR-DEFIB
PHYSIO-CONTROL, INC.
99400
Not in Commercial Distribution

  • 00721902152962 ()
99400-000822

  • Physiologic-monitoring defibrillation system

LIFEPAK® 12 defibrillator/monitor - 00721902151491

LP12AABBABABBABAAAAAAAAALP12 MONITOR-DEFIB
PHYSIO-CONTROL, INC.
99400
Not in Commercial Distribution

  • 00721902151491 ()
99400-000675

  • Physiologic-monitoring defibrillation system

LIFEPAK® 12 defibrillator/monitor - 00721902150937

LP12AAABABAABBABAAAAAAAALP12 MONITOR-DEFIB
PHYSIO-CONTROL, INC.
99400
Not in Commercial Distribution

  • 00721902150937 ()
99400-000619

  • Physiologic-monitoring defibrillation system
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