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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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Amplatz Type Renal Sheath Set
BOSTON SCIENTIFIC CORPORATION
M0062601500
In Commercial Distribution

  • 08714729005568 ()

  • 24 F Diameter
  • 30 F Diameter
  • 10.1 mm Diameter
  • 8.1 mm Diameter


  • Multi-purpose percutaneous abdominothoracic drainage catheter
The FFX implant is a sterile, single patient use, long-term implantable devices consisting of a D-shaped cage made of titanium with an oval shape that is designed to be filled with bone graft. The top and bottom surfaces of the cage have sawtooth-shaped surface to improve fixation to the bone.
SC MEDICA
57.000.60S
In Commercial Distribution

  • 03770019503058 ()


  • Spinal bone screw, non-bioabsorbable
The FFX implant is a sterile, single patient use, long-term implantable devices consisting of a D-shaped cage made of titanium with an oval shape that is designed to be filled with bone graft. The top and bottom surfaces of the cage have sawtooth-shaped surface to improve fixation to the bone.
SC MEDICA
57.000.50S
In Commercial Distribution

  • 03770019503041 ()


  • Spinal bone screw, non-bioabsorbable
The FFX implant is a sterile, single patient use, long-term implantable devices consisting of a D-shaped cage made of titanium with an oval shape that is designed to be filled with bone graft. The top and bottom surfaces of the cage have sawtooth-shaped surface to improve fixation to the bone.
SC MEDICA
57.000.40S
In Commercial Distribution

  • 03770019503034 ()


  • Spinal bone screw, non-bioabsorbable
The FFX implant is a sterile, single patient use, long-term implantable devices consisting of a D-shaped cage made of titanium with an oval shape that is designed to be filled with bone graft. The top and bottom surfaces of the cage have sawtooth-shaped surface to improve fixation to the bone.
SC MEDICA
57.000.30S
In Commercial Distribution

  • 03770019503027 ()


  • Spinal bone screw, non-bioabsorbable
The FFX implant is a sterile, single patient use, long-term implantable devices consisting of a D-shaped cage made of titanium with an oval shape that is designed to be filled with bone graft. The top and bottom surfaces of the cage have sawtooth-shaped surface to improve fixation to the bone.
SC MEDICA
57.000.20S
In Commercial Distribution

  • 03770019503010 ()


  • Spinal bone screw, non-bioabsorbable
The FFX implant is a sterile, single patient use, long-term implantable devices consisting of a D-shaped cage made of titanium with an oval shape that is designed to be filled with bone graft. The top and bottom surfaces of the cage have sawtooth-shaped surface to improve fixation to the bone.
SC MEDICA
57.000.10S
In Commercial Distribution

  • 03770019503003 ()


  • Spinal bone screw, non-bioabsorbable
An implantable short tube intended to provide a bypass route for tear drainage from the corner of the eye into the nasal cavity, or a paranasal sinus, as treatment for pathologies of the tear drainage system in association with functional or obstructive epiphora; it may also be intended to facilitate saline solution irrigation to a paranasal sinus (e.g., ethmoid sinus) to manage chronic rhinosinusitis. Also referred to as a lacrimal stent (e.g., Lester Jones type), it is implanted after surgery to dilate or maintain a surgically-created passage [e.g., dacryocystostomy/dacryocystorhinostomy (DCR)], and is made of glass or synthetic polymer materials (e.g., silicone).
FCI S A S FCI 20 22
S1.1495
In Commercial Distribution

  • 33760087127271 ()
  • 03760087127270 ()
  • 13760087127277 ()


  • Lacrimal tube
An implantable short tube intended to provide a bypass route for tear drainage from the corner of the eye into the nasal cavity, or a paranasal sinus, as treatment for pathologies of the tear drainage system in association with functional or obstructive epiphora; it may also be intended to facilitate saline solution irrigation to a paranasal sinus (e.g., ethmoid sinus) to manage chronic rhinosinusitis. Also referred to as a lacrimal stent (e.g., Lester Jones type), it is implanted after surgery to dilate or maintain a surgically-created passage [e.g., dacryocystostomy/dacryocystorhinostomy (DCR)], and is made of glass or synthetic polymer materials (e.g., silicone).
FCI S A S FCI 20 22
S1.1455
In Commercial Distribution

  • 33760087127264 ()
  • 03760087127263 ()
  • 13760087127260 ()


  • Lacrimal tube
FCI NUNCHAKU 105
FCI S A S FCI 20 22
S1.1371
In Commercial Distribution

  • 13760087123743 ()
  • 03760087123746 ()


  • Lacrimal tube
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