SEARCH RESULTS FOR: (*Fake Texas A*)(9274 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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CARDINAL HEALTH - 10197106832615

SPINE PACK
Cardinal Health 200, LLC
SNE48LMCO4
In Commercial Distribution

  • 50197106832613 ()
  • 10197106832615 ()
SNE48LMCO4

  • Ice bag

CARDINAL HEALTH - 10197106733257

D AND C PACK
Cardinal Health 200, LLC
SMA69DPHEE
In Commercial Distribution

  • 50197106733255 ()
  • 10197106733257 ()
SMA69DPHEE

  • Obstetrical/gynaecological surgical procedure kit, medicated

CARDINAL HEALTH - 10197106744598

PULL D C PACK
Cardinal Health 200, LLC
09-7335A
In Commercial Distribution

  • 50197106744596 ()
  • 10197106744598 ()
09-7335A

  • Obstetrical/gynaecological surgical procedure kit, medicated

CARDINAL HEALTH - 10197106743270

EXTREMITY PACK
Cardinal Health 200, LLC
SOP69EPOCA
In Commercial Distribution

  • 50197106743278 ()
  • 10197106743270 ()
SOP69EPOCA

  • Orthopaedic surgical procedure kit, non-medicated, single-use

CARDINAL HEALTH - 10197106742211

SHOULDER PACK
Cardinal Health 200, LLC
SOP45SPSTA
In Commercial Distribution

  • 50197106742219 ()
  • 10197106742211 ()
SOP45SPSTA

  • Orthopaedic surgical procedure kit, medicated

CARDINAL HEALTH - 10197106736715

KIT, D C D E
Cardinal Health 200, LLC
PBOCDCBLI
In Commercial Distribution

  • 50197106736713 ()
  • 10197106736715 ()
PBOCDCBLI

  • Obstetrical/gynaecological surgical procedure kit, medicated

CARDINAL HEALTH - 10197106756478

HAND PACK 2
Cardinal Health 200, LLC
SOP56HKSJA
In Commercial Distribution

  • 50197106756476 ()
  • 10197106756478 ()
SOP56HKSJA

  • Orthopaedic surgical procedure kit, medicated

CARDINAL HEALTH - 10197106804599

D AND C PACK
Cardinal Health 200, LLC
SMA29DCPCH
In Commercial Distribution

  • 50197106804597 ()
  • 10197106804599 ()
SMA29DCPCH

  • Obstetrical/gynaecological surgical procedure kit, medicated

UroShield 3.0 Driver - 07290103420277

The UroShield driver is an electronic unit intended to drive an accessory (Ultrasonic Actuator) that creates surface acoustic waves on Urinary catheter to prevent bacterial adhesion and minimized risk of CAUTI (Catheter Associated Urinary Tract Infections).
NANOVIBRONIX INC.
3.0
In Commercial Distribution

  • 07290103420277 ()
10-800-0003

  • Urinary catheter ultrasonic bacterial adhesion inhibition system

UroShield Kit - 07290103420260

The UroShield device is a single-patient, extracorporeal accessory to indwelling urinary catheters consisting of a disposable Actuator and a reusable Driver. After the Foley catheter is placed in the patient, the disposable Actuator is clipped on the extracorporeal part of the catheter and then connected to the reusable Driver through the Actuator’s cable connector and Driver’s cable socket connection. When the Driver is turned on, the Actuator creates surface acoustic waves that propagate on the catheter surface. The UroShield surface acoustic waves reduce bacterial adhesion on the catheter surface, thereby designed to minimize the risk of CAUTI (Catheter-Associated Urinary Tract Infections).
NANOVIBRONIX INC.
3.0
In Commercial Distribution

  • 07290103420260 ()
10-200-0004

  • Urinary catheter ultrasonic bacterial adhesion inhibition system
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