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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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Timberline® MPF Lateral Interbody Modular Plate Fixation System - 00887868199271

No Description
BIOMET SPINE LLC
8615-5514
In Commercial Distribution

  • 00887868199271 ()

  • SPACER MPF PEEK 0DEG 55L X 26W X 14HMM
8615-5514

  • Polymeric spinal interbody fusion cage

Timberline® MPF Lateral Interbody Modular Plate Fixation System - 00887868199264

No Description
BIOMET SPINE LLC
8615-5512
In Commercial Distribution

  • 00887868199264 ()

  • SPACER MPF PEEK 0DEG 55L X 26W X 12HMM
8615-5512

  • Polymeric spinal interbody fusion cage

Timberline® MPF Lateral Interbody Modular Plate Fixation System - 00887868199257

No Description
BIOMET SPINE LLC
8615-5510
In Commercial Distribution

  • 00887868199257 ()

  • SPACER MPF PEEK 0DEG 55L X 26W X 10HMM
8615-5510

  • Polymeric spinal interbody fusion cage

Timberline® MPF Lateral Interbody Modular Plate Fixation System - 00887868199585

No Description
BIOMET SPINE LLC
8616-6016
In Commercial Distribution

  • 00887868199585 ()

  • SPACER MPF PEEK 8DEG 60L X 26W X 16HMM
8616-6016

  • Polymeric spinal interbody fusion cage

Timberline® MPF Lateral Interbody Modular Plate Fixation System - 00887868199578

No Description
BIOMET SPINE LLC
8616-6014
In Commercial Distribution

  • 00887868199578 ()

  • SPACER MPF PEEK 8DEG 60L X 26W X 14HMM
8616-6014

  • Polymeric spinal interbody fusion cage

Timberline® MPF Lateral Interbody Modular Plate Fixation System - 00887868199370

No Description
BIOMET SPINE LLC
8616-4014
In Commercial Distribution

  • 00887868199370 ()

  • SPACER MPF PEEK 8DEG 40L X 26W X 14HMM
8616-4014

  • Polymeric spinal interbody fusion cage

Timberline® MPF Lateral Interbody Modular Plate Fixation System - 00887868199363

No Description
BIOMET SPINE LLC
8616-4012
In Commercial Distribution

  • 00887868199363 ()

  • SPACER MPF PEEK 8DEG 40L X 26W X 12HMM
8616-4012

  • Polymeric spinal interbody fusion cage

Timberline® MPF Lateral Interbody Modular Plate Fixation System - 00887868199356

No Description
BIOMET SPINE LLC
8616-4010
In Commercial Distribution

  • 00887868199356 ()

  • SPACER MPF PEEK 8DEG 40L X 26W X 10HMM
8616-4010

  • Polymeric spinal interbody fusion cage

Prometra Physician Configuration Device - 00810335020181

The Physician Configuration Device is used to configure the Patient Therapy Controller for proper use with a single Programmable Pump. It can also be used to read historical data and error logs from the Patient Therapy Controller.
Flowonix Medical, Inc.
12861
In Commercial Distribution

  • 00810335020181 ()


  • Infusion pump programmer

LimFlow Extension Stent Graft - 00850041730219

LimFlow Extension Stent Graft (5.5 mm x 200 mm). The LimFlow Extension Stent Graft is indicated for patients who have chronic limb-threatening ischemia with no suitable endovascular or surgical revascularization options and are at risk of major amputation.
Limflow Inc.
RGS-55200-US-24
In Commercial Distribution

  • 00850041730219 ()


  • Arteriovenous endovascular stent-graft
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