SEARCH RESULTS FOR: 仿制AT(7976 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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Everolimus-Eluting Platinum Chromium Coronary Stent System
BOSTON SCIENTIFIC CORPORATION
H7493925208250
In Commercial Distribution

  • 08714729828747 ()

  • 2.50 mm Stent Diameter
  • 8 mm Stent Length
H7493925208250

  • Coronary angioplasty balloon catheter, basic
  • Drug-eluting coronary artery stent, non-bioabsorbable-polymer-coated
Everolimus-Eluting Platinum Chromium Coronary Stent System
BOSTON SCIENTIFIC CORPORATION
H7493925208220
In Commercial Distribution

  • 08714729828730 ()

  • 8 mm Stent Length
  • 2.25 mm Stent Diameter
H7493925208220

  • Coronary angioplasty balloon catheter, basic
  • Drug-eluting coronary artery stent, non-bioabsorbable-polymer-coated
Everolimus-Eluting Platinum Chromium Coronary Stent System
BOSTON SCIENTIFIC CORPORATION
H7493911432250
Not in Commercial Distribution

  • 08714729823681 ()

  • 2.50 mm Stent Diameter
  • 32 mm Stent Length
H7493911432250

  • Drug-eluting coronary artery stent, non-bioabsorbable-polymer-coated
  • Coronary angioplasty balloon catheter, basic
Cable Set
BOSTON SCIENTIFIC CORPORATION
M004PF61M499D
In Commercial Distribution

  • 00191506052447 ()
M004PF61M499D

  • Electrocardiographic lead set, reusable
  • Electrical-only medical device connection cable, reusable
The NeuroPace® Patient Data Management System (PDMS), part of the NeuroPace® RNS® System, is used to store and provide access to historical RNS® Neurostimulator and patient data. The PDMS can also be used to create and simulate detection settings that can be sent to a user identified NeuroPace® Programmer for use at a later date. PDMS is stand-alone software that is accessible via secure internet connection.
Neuropace, Inc.
Model 4340
In Commercial Distribution

  • 00855547005007 ()


  • Cannulated surgical drill bit, reusable
Prolapse Repair System - Posterior
Coloplast A/S
50150
In Commercial Distribution

  • 05708932459433 ()
50150

  • Suturing unit, single-use
  • Female stress urinary incontinence surgical mesh-sling, synthetic polymer
Prolapse Repair System - Anterior
Coloplast A/S
50100
In Commercial Distribution

  • 05708932459457 ()
50100

  • Suturing unit, single-use
  • Female stress urinary incontinence surgical mesh-sling, synthetic polymer
Coronary Stent System
BOSTON SCIENTIFIC CORPORATION
H7493893532500
Not in Commercial Distribution

  • 08714729471417 ()

  • 32 mm Stent Length
  • 5.0 mm Stent Diameter
H7493893532500

  • Coronary angioplasty balloon catheter, basic
  • Bare-metal coronary artery stent
Coronary Stent System
BOSTON SCIENTIFIC CORPORATION
H7493893532450
Not in Commercial Distribution

  • 08714729471400 ()

  • 32 mm Stent Length
  • 4.5 mm Stent Diameter
H7493893532450

  • Bare-metal coronary artery stent
  • Coronary angioplasty balloon catheter, basic
Coronary Stent System
BOSTON SCIENTIFIC CORPORATION
H7493893528500
Not in Commercial Distribution

  • 08714729471394 ()

  • 5.0 mm Stent Diameter
  • 28 mm Stent Length
H7493893528500

  • Bare-metal coronary artery stent
  • Coronary angioplasty balloon catheter, basic
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