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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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Pacifica/Ventura MIS Inserter, 20 Deg
Seaspine Orthopedics Corporation
93-3492
In Commercial Distribution

  • 10889981088934 ()

  • 20 Deg
93-3492

  • Orthopaedic inorganic implant inserter/extractor, reusable
No Description
Biomet Orthopedics, LLC
IFI-491422
In Commercial Distribution

  • 00880304826588 ()

  • 20 MM
IFI-491422

  • Implant handling forceps, scissors-like
NAMIC Angiographic 20 ml Control Syringe
NAVILYST MEDICAL, INC.
80075027
In Commercial Distribution

  • H749800750271 ()
  • H749800750270 ()

  • 20 ml


  • Angiographic syringe
NAMIC Angiographic 20 ml Control Syringe
NAVILYST MEDICAL, INC.
80075023
In Commercial Distribution

  • H749800750231 ()
  • H749800750230 ()

  • 20 ml


  • Angiographic syringe
TRIAL, NECK, 16/20, STANDARD, REVISION STEM
Exactech, Inc.
01-011-00-1620
In Commercial Distribution

  • 10885862286215 ()

  • 60/20
01-011-00-1620

  • Femoral stem prosthesis trial
TRIAL, NECK, EXTENDED OFFSET, SIZE 20
Exactech, Inc.
161-23-20
In Commercial Distribution

  • 10885862034632 ()

  • SIZE 20
161-23-20

  • Femoral stem prosthesis trial
TRIAL, NECK, STANDARD OFFSET, SIZE 20
Exactech, Inc.
161-22-20
In Commercial Distribution

  • 10885862034540 ()

  • SIZE 20
161-22-20

  • Femoral stem prosthesis trial
Flex Hinge Toe Sizer, Lateral
WRIGHT MEDICAL TECHNOLOGY, INC.
4460120
In Commercial Distribution

  • 00840420189837 ()

  • Size: 2-0
4460120

  • Surgical implant template, reusable
Bone Graft Instrument Set - Posterior 20° Glenoid Stopper Jig
LIMACORPORATE SPA
Bone Graft Instrument Set
In Commercial Distribution

  • 08033390109598 ()

  • Posterior 20°
9013.75.436

  • Orthopaedic reamer guide
A hollow cylinder inserted orally or nasally into the trachea to provide an unobstructed airway to convey gases and vapours to and from the lungs during anaesthesia, resuscitation, and other situations where the patient is not properly ventilated. The device may: 1) be packaged with a connector that will attach to a breathing circuit or manual resuscitator; 2) have a distal inflatable cuff to seal against the tracheal wall; 3) be radiopaque; and 4) have a built-in pilot balloon for cuff pressure monitoring. It is typically made of plastic or rubber and is available in various diameters and lengths for adult and paediatric patients. This is a single-use device.
FORSURE MEDICAL PRODUCTS LLC
11210050
In Commercial Distribution

  • 20815123011918 ()
  • 10815123011911 ()
  • 00815123011914 ()

  • 20 Fr
  • Lumen/Inner Diameter: 5.0 Millimeter
11210050

  • Basic endotracheal tube, single-use
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