SEARCH RESULTS FOR: 购买假的单位存款证明【咨询网:ｚｊｗ２１１.ｃｏｍ】宜城得克萨斯A(72107 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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Safire™ Blu™ SP - 05414734310758

Ablation Catheter
IRVINE BIOMEDICAL, INC.
A402870
Not in Commercial Distribution

  • 05414734310758 ()

  • Catheter Gauge: 7 French
A402870

  • Cardiac radio-frequency ablation system catheter

SJM™ - 05414734308847

Electrophysiology Cable
IRVINE BIOMEDICAL, INC.
IBI-85711
In Commercial Distribution

  • 05414734308847 ()

  • Length: 8 Feet
IBI-85711

  • Electrical-only medical device connection cable, reprocessed

SJM™ - 05414734308755

Electrophysiology Cable
IRVINE BIOMEDICAL, INC.
IBI-85641
In Commercial Distribution

  • 05414734308755 ()

  • Length: 8 Feet
IBI-85641

  • Electrical-only medical device connection cable, reprocessed

PASCAL - 00690103216981

PASCAL TABLE US COMMERCIAL
Edwards Lifesciences LLC
10000T
In Commercial Distribution

  • 00690103216981 ()
10000TA

  • Cardiac implantation catheter table

PASCAL - 00690103216974

PASCAL SYSTEM - STABILIZER RAIL SYSTEM
Edwards Lifesciences LLC
20000ST
In Commercial Distribution

  • 00690103216974 ()
20000STA

  • Cardiac implantation catheter holder

PASCAL PRECISION - 00690103216967

PASCAL PRECISION SYSTEM - GUIDE SHEATH
Edwards Lifesciences LLC
20000GSA
In Commercial Distribution

  • 00690103216967 ()
20000GSA

  • Heart valve clip

PASCAL - 00690103216950

PASCAL PRECISION SYSTEM – PASCAL ACE IMPLANT SYSTEM
Edwards Lifesciences LLC
20000ISM
In Commercial Distribution

  • 00690103216950 ()
20000ISMA

  • Heart valve clip

PASCAL - 00690103216943

PASCAL PRECISION SYSTEM – IMPLANT SYSTEM
Edwards Lifesciences LLC
20000IS
In Commercial Distribution

  • 00690103216943 ()
20000ISA

  • Heart valve clip

TORUS Stent Graft System - 00860008946478

The DETOUR System is indicated for use for percutaneous revascularization in patients with symptomatic femoropopliteal lesions from 200 mm to 460 mm in length with chronic total occlusions (100 mm to 425 mm) or diffuse stenosis >70% who may be considered suboptimal candidates for surgical or alternative endovascular treatments. The DETOUR System, or any of its components, is not for use in the coronary and cerebral vasculature
PQ Bypass, Inc.
TSG-6.7X200
In Commercial Distribution

  • 00860008946478 ()

  • 6.7mm Stent Graft Proximal Diameter
  • 6.7mm Stent Graft Distal Diameter
  • 135cm Catheter Working Length
  • 8F Delivery System Outer Profile
  • 200mm Covered Stent Graft Length
TSG-6.7X200

  • Central/peripheral venous endovascular stent-graft

TORUS Stent Graft System - 00860008946461

The DETOUR System is indicated for use for percutaneous revascularization in patients with symptomatic femoropopliteal lesions from 200 mm to 460 mm in length with chronic total occlusions (100 mm to 425 mm) or diffuse stenosis >70% who may be considered suboptimal candidates for surgical or alternative endovascular treatments. The DETOUR System, or any of its components, is not for use in the coronary and cerebral vasculature
PQ Bypass, Inc.
TSG-6.7X150
In Commercial Distribution

  • 00860008946461 ()

  • 6.7mm Stent Graft Proximal Diameter
  • 6.7mm Stent Graft Distal Diameter
  • 135cm Catheter Working Length
  • 8F Delivery System Outer Profile
  • 150mm Covered Stent Graft Length
TSG-6.7X150

  • Central/peripheral venous endovascular stent-graft
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