SEARCH RESULTS FOR: (*Union Institute*)(7006 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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Integra® Miltex® - 10381780360179

Integra® Miltex® Bakes Common Duct Dilator, 8-1/2", 5mm Diameter
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
14-10-5
In Commercial Distribution

  • H834141051 ()
  • 10381780360179 ()
14-10-5

  • Common bile duct dilator

Integra® Miltex® - 10381780360162

Integra® Miltex® Bakes Common Duct Dilator, 8-1/2", 4mm Diameter
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
14-10-4
In Commercial Distribution

  • H834141041 ()
  • 10381780360162 ()
14-10-4

  • Common bile duct dilator

Integra® Miltex® - 10381780360155

Integra® Miltex® Bakes Common Duct Dilator, 8-1/2", 3mm Diameter
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
14-10-3
In Commercial Distribution

  • H834141031 ()
  • 10381780360155 ()
14-10-3

  • Common bile duct dilator

Integra® Miltex® - 10381780360148

Integra® Miltex® Bakes Common Duct Dilator, 8-1/2", 11mm Diameter
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
14-10-11
In Commercial Distribution

  • H8341410111 ()
  • 10381780360148 ()
14-10-11

  • Common bile duct dilator

Integra® Miltex® - 10381780360131

Integra® Miltex® Bakes Common Duct Dilator, 8-1/2", 10mm Diameter
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
14-10-10
In Commercial Distribution

  • H8341410101 ()
  • 10381780360131 ()
14-10-10

  • Common bile duct dilator

CMF - 00888912011495

The SpinaLogic is a portable, battery powered, microcontrolled, noninvasive bone growth stimulator indicated as an adjunct electrical treatment to primary lumbar spinal fusion surgery for one or two levels. The SpinaLogic is available in one size.
DJO, LLC
Spinalogic
In Commercial Distribution

  • 00888912011495 ()
01-207-0007

  • Patient-worn bone growth electromagnetic stimulator

CMF - 00888912011488

The OL1000 and OL1000 SC BONE GROWTH STIMULATORS are indicated for the noninvasive treatment of an established nonunion acquired secondary to trauma, excluding vertebrae and all flat bones. A nonunion is considered to be established when the fracture site shows no visibly progressive signs of healing. The OL1000 and OL1000 SC are portable, battery powered, microprocessor-controlled, noninvasive bone growth stimulators. The device is worn by a patient for 30 minutes a day and provides local electromagnetic field treatment for a non-healing fracture. The device produces very low energy combined static and dynamic electromagnetic fields on the order of the earth’s magnetic field. The device has a push button that starts the treatment and an audible tone to notify the patient that a treatment has started or has ended. A liquid crystal display (LCD) is utilized to display the status of the device, e.g., treatment record, daily treatment time countdown.
DJO, LLC
OL1000 Dual Coil
In Commercial Distribution

  • 00888912011488 ()
01-203-0001

  • Patient-worn bone growth electromagnetic stimulator

Accelstim - 08050040997336

Replacement Aquasonics 100 Ultrasound Gel, AccelStim 4300
IGEA SPA
UBHS-02
In Commercial Distribution

  • 08050040997336 ()
654300-9002

  • Bone growth ultrasonic stimulator

Accelstim - 08050040997329

Replacement Power Supply, Accelstim 4300
IGEA SPA
UBHS-02
In Commercial Distribution

  • 08050040997329 ()
654300-9003

  • Bone growth ultrasonic stimulator

Accelstim - 08050040997312

Replacement Transducer Holder, Accelstim 4300
IGEA SPA
UBHS-02
In Commercial Distribution

  • 08050040997312 ()
654300-8002

  • Bone growth ultrasonic stimulator
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