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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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Coronary Stent System
BOSTON SCIENTIFIC CORPORATION
H7493893524400
Not in Commercial Distribution

  • 08714729396222 ()

  • 4.0 mm Stent Diameter
  • 24 mm Stent Length
H7493893524400

  • Bare-metal coronary artery stent
  • Coronary angioplasty balloon catheter, basic
Coronary Stent System
BOSTON SCIENTIFIC CORPORATION
H7493893524270
Not in Commercial Distribution

  • 08714729396192 ()

  • 24 mm Stent Length
  • 2.75 mm Stent Diameter
H7493893524270

  • Bare-metal coronary artery stent
  • Coronary angioplasty balloon catheter, basic
Coronary Stent System
BOSTON SCIENTIFIC CORPORATION
H7493893520500
Not in Commercial Distribution

  • 08714729396161 ()

  • 20 mm Stent Length
  • 5.0 mm Stent Diameter
H7493893520500

  • Coronary angioplasty balloon catheter, basic
  • Bare-metal coronary artery stent
Guide Wire for Percutaneous Leads
ST. JUDE MEDICAL, INC.
1102
In Commercial Distribution

  • 15414734400029 ()
  • 05414734400022 ()
1102

  • Spinal guidewire
The Micro USB Cable is used to charge Eversense Transmitter
SENSEONICS, INCORPORATED
FG-6000-01-302
In Commercial Distribution

  • 00817491023841 ()


  • Implantable glucose monitoring system transmitter
No Description
PREMIA SPINE LTD
88020
In Commercial Distribution

  • 07290115935110 ()


  • Spinal guidewire
No Description
PREMIA SPINE LTD
87865
In Commercial Distribution

  • 07290115935042 ()


  • Spinal guidewire
No Description
PREMIA SPINE LTD
87359
In Commercial Distribution

  • 07290115934854 ()


  • Spinal guidewire
No Description
PREMIA SPINE LTD
87271
In Commercial Distribution

  • 07290115934786 ()


  • Spinal guidewire
No Description
PREMIA SPINE LTD
87010
In Commercial Distribution

  • 07290115934687 ()


  • Spinal guidewire
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