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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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AngioSculpt® PTCA Scoring Balloon Catheter - M370200130201

No Description
Angioscore Inc.
2001-3020
In Commercial Distribution

  • M370200130201 ()


  • Coronary angioplasty balloon catheter, basic

AngioSculpt® PTCA Scoring Balloon Catheter - M3702001301510

No Description
Angioscore Inc.
2001-3015
In Commercial Distribution

  • M3702001301510 ()


  • Coronary angioplasty balloon catheter, basic

AngioSculpt® PTCA Scoring Balloon Catheter - M370200130101

No Description
Angioscore Inc.
2001-3010
In Commercial Distribution

  • M370200130101 ()


  • Coronary angioplasty balloon catheter, basic

AngioSculpt® PTCA Scoring Balloon Catheter - M3702001252010

No Description
Angioscore Inc.
2001-2520
In Commercial Distribution

  • M3702001252010 ()


  • Coronary angioplasty balloon catheter, basic

AngioSculpt® PTCA Scoring Balloon Catheter - M3702001251514

No Description
Angioscore Inc.
2001-2515
In Commercial Distribution

  • M3702001251514 ()


  • Coronary angioplasty balloon catheter, basic

AngioSculpt® PTCA Scoring Balloon Catheter - M370200125101

No Description
Angioscore Inc.
2001-2510
In Commercial Distribution

  • M370200125101 ()


  • Coronary angioplasty balloon catheter, basic

AngioSculpt® PTCA Scoring Balloon Catheter - M370200120201

No Description
Angioscore Inc.
2001-2020
In Commercial Distribution

  • M370200120201 ()


  • Coronary angioplasty balloon catheter, basic

AngioSculpt® PTCA Scoring Balloon Catheter - M370200120151

No Description
Angioscore Inc.
2001-2015
In Commercial Distribution

  • M370200120151 ()


  • Coronary angioplasty balloon catheter, basic

AngioSculpt® PTCA Scoring Balloon Catheter - M370200120101

No Description
Angioscore Inc.
2001-2010
In Commercial Distribution

  • M370200120101 ()


  • Coronary angioplasty balloon catheter, basic

PROMUS Element™ Plus - 08714729807742

Everolimus-Eluting Platinum Chromium Coronary Stent System
BOSTON SCIENTIFIC CORPORATION
H7493911608400
Not in Commercial Distribution

  • 08714729807742 ()

  • 8 mm Stent Length
  • 4.00 mm Stent Diameter
H7493911608400

  • Drug-eluting coronary artery stent, non-bioabsorbable-polymer-coated
  • Coronary angioplasty balloon catheter, basic
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