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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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GLIDESHEATH SLENDER Hydrophobic Coated Introducer Sheath
TERUMO CORPORATION
RM*ES6J16HAT
Not in Commercial Distribution

  • 34987350717963 ()
  • 04987350717962 ()
  • 54987350717967 ()

  • Those Clinically Relevant Size are relative to the sheath.
  • Length: 16 Centimeter
  • Lumen/Inner Diameter: 2.10 Millimeter
RM*ES6J16HAT

  • Vascular catheter introduction set, nonimplantable
GLIDESHEATH SLENDER Hydrophobic Coated Introducer Sheath
TERUMO CORPORATION
RM*ES6J10HAT
Not in Commercial Distribution

  • 34987350717949 ()
  • 04987350717948 ()
  • 54987350717943 ()

  • Lumen/Inner Diameter: 2.10 Millimeter
  • Those Clinically Relevant Size are relative to the sheath.
  • Length: 10 Centimeter
RM*ES6J10HAT

  • Vascular catheter introduction set, nonimplantable
WIRE/PIN CUTTER DOUBLE ACTION ANGLED TUNGSTEN CARBIDE BLADES
SONTEC INSTRUMENTS, INC.
1103-103V
In Commercial Distribution

  • 00192896051447 ()

  • 30 Degree Tip
  • For wire up to 2.2 Millimeter
  • Length: 8.75 Inch
1103-103V

  • Orthopaedic implantable-device cutter
WIRE/PIN CUTTER DOUBLE ACTION ANGLED TUNGSTEN CARBIDE BLADES
SONTEC INSTRUMENTS, INC.
1103-102
In Commercial Distribution

  • 00192896051430 ()

  • 15 Degree Tip
  • For wire up to 2.2 Millimeter
  • Length: 8.75 Inch
1103-102

  • Orthopaedic implantable-device cutter
Forehead SpO2 Sensor
Covidien LP
MAXFASTI
In Commercial Distribution

  • 20884521815466 ()
  • 10884521815469 ()

  • Patient Weight, Greater than or Equal to 10, KG;


  • Pulse oximeter probe, single-use
Forehead SpO2 Sensor
Covidien LP
MAXFAST
In Commercial Distribution

  • 20884521815367 ()
  • 10884521815360 ()

  • Patient Weight, Greater than or Equal to 10, KG;


  • Pulse oximeter probe, single-use
Forehead SpO2 Sensor
Covidien LP
MAXFAST
In Commercial Distribution

  • 20884522039717 ()
  • 10884522039710 ()

  • Patient Weight, Greater than or Equal to 10, KG;


  • Pulse oximeter probe, single-use
No Description
BIOMET SPINE LLC
14-525256E
In Commercial Distribution

  • 00880304982949 ()

  • 8.0 x 56 mm Cross-Connector Head to Head Cross-Connector
14-525256E

  • Bone-screw internal spinal fixation system, sterile
No Description
BIOMET SPINE LLC
14-525249E
In Commercial Distribution

  • 00880304982932 ()

  • 8.0 x 49 mm Cross-Connector Head to Head Cross-Connector
14-525249E

  • Bone-screw internal spinal fixation system, sterile
No Description
BIOMET SPINE LLC
14-525242E
In Commercial Distribution

  • 00880304982925 ()

  • 8.0 x 42 mm Cross-Connector Head to Head Cross-Connector
14-525242E

  • Bone-screw internal spinal fixation system, sterile
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