SEARCH RESULTS FOR: ("Make Dominican School of Philosophy")(70002 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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TORUS Stent Graft System - 00860008946454

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-6.7X100
In Commercial Distribution

  • 00860008946454 ()

  • 6.7mm Stent Graft Proximal Diameter
  • 6.7mm Stent Graft Distal Diameter
  • 135cm Catheter Working Length
  • 8F Delivery System Outer Profile
  • 100mm Covered Stent Graft Length
TSG-6.7X100

  • Central/peripheral venous endovascular stent-graft

TORUS Stent Graft System - 00860008946447

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-6.0X200
In Commercial Distribution

  • 00860008946447 ()

  • 6.0 mm Stent Graft Proximal Diameter
  • 6.0 mm Stent Graft Distal Diameter
  • 135cm Catheter Working Length
  • 6F Delivery System Outer Profile
  • 200mm Covered Stent Graft Length
TSG-6.0X200

  • Central/peripheral venous endovascular stent-graft

TORUS Stent Graft System - 00860008946430

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-6.0X150
In Commercial Distribution

  • 00860008946430 ()

  • 6.0mm Stent Graft Proximal Diameter
  • 6.0mm Stent Graft Distal Diameter
  • 135cm Catheter Working Length
  • 8F Delivery System Outer Profile
  • Covered Stent Graft Length
TSG-6.0X150

  • Central/peripheral venous endovascular stent-graft

TORUS Stent Graft System - 00860008946423

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-6.0X100
In Commercial Distribution

  • 00860008946423 ()

  • 6.0 mm Stent Graft Proximal Diameter
  • 6.0 mm Stent Graft Distal Diameter
  • 135cm Catheter Working Length
  • 8F Delivery System Outer Profile
  • 100 mm Covered Stent Graft Length
TSG-6.0X100

  • Central/peripheral venous endovascular stent-graft

TORUS Stent Graft System - 00860008946416

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-5.5X200
In Commercial Distribution

  • 00860008946416 ()

  • 5.5 mm Stent Graft Proximal Diameter
  • 5.5 mm Stent Graft Distal Diameter
  • 135cm Catheter Working Length
  • 8F Delivery System Outer Profile
  • 200 mm Covered Stent Graft Length
TSG-5.5X200

  • Central/peripheral venous endovascular stent-graft

ENDOCROSS Device - 00860008946409

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.
ENDOCROSS
In Commercial Distribution

  • 00860008946409 ()
ENDOCROSS

  • Vascular guide-catheter, single-use

NA - 10886704078845

Models 400 and 550 Implantable Infusion Pump Refill Kit Contents: (1) 50 ml Calibrated Syringe Barrel (1) Tubing Set with Removable Injection Site (1) Stopcock (2) Huber Point Needles 22 Gauge x 1inch (2.54 cm) (2) Huber Point Needles 22 Gauge x 1.5inch (3.8 cm) (6) Gauze Pads (1) Fenestrated Drape (2) Pump Templates (2) Adhesive Bandages (1) Refill Worksheet (1) Set of INSTRUCTIONS FOR USE
Medos International Sàrl
IP40820US
Not in Commercial Distribution

  • 10886704078845 ()
IP40820US

  • Implantable intrathecal infusion pump, nonprogrammable

Belotero Balance (+) Lidocaine - 07640123791343

Belotero Balance (+) Lidocaine is a hyaluronic-acid based dermal filler approved for injection into the mid-to-deep dermis for correction of moderate-to-severe facial wrinkles and folds, such as nasolabial folds. The device is a kitted pack containing: (1) a pre-filled, sterile Belotero Balance (+) Lidocaine gel in a 1 mL syringe, (2) two sterile needles (27G x 1/2, 30G x 1/2), and (3) two patient record labels
ANTEIS SA
8710M0S
In Commercial Distribution

  • 07640123791343 ()

  • Total Volume: 1.0 Milliliter
  • Needle Gauge: 27 Gauge
  • Needle Gauge: 30 Gauge


  • Dermal tissue reconstructive material, microbe-derived, anaesthetic

Belotero Balance - 07640123791213

Belotero Balance is a hyaluronic-acid based dermal filler approved for injection into the mid-to-deep dermis for correction of moderate-to-severe facial wrinkles and folds, such as nasolabial folds. The device is a kitted pack containing: (1) a pre-filled, sterile Belotero Balance gel in a 1 mL syringe, (2) two sterile needles (27G x 1/2 in, 30G x 1/2 in), and (3) two patient record labels.
ANTEIS SA
8700M0S
In Commercial Distribution

  • 07640123791213 ()

  • Needle Gauge: 27 Gauge
  • Needle Gauge: 30 Gauge
  • Total Volume: 1 Milliliter


  • Dermal tissue reconstructive material, microbe-derived

Belotero Balance - 07640123791152

Belotero Balance is a hyaluronic-acid based dermal filler approved for injection into the mid-to-deep dermis for correction of moderate-to-severe facial wrinkles and folds, such as nasolabial folds. The device is a kitted pack containing: (1) a pre-filled, sterile Belotero Balance gel in a 1 mL syringe, (2) two sterile needles (27G x 1/2 in, 30G x 1/2 in), and (3) two patient record labels.
ANTEIS SA
8706M0
In Commercial Distribution

  • 07640123791152 ()

  • Total Volume: 1 Milliliter
  • Needle Gauge: 27 Gauge
  • Needle Gauge: 30 Gauge


  • Dermal tissue reconstructive material, microbe-derived
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