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Simpulse™ Pulse lavage Simpulse™ VariCare™ Suction Irrigator

Simpulse™ VariCare™ Suction Irrigator

Overview

For Enhanced Wound Management

Simpulse™ VariCare™ provides controlled powered irrigation for the cleansing and debridement of burns and wounds.

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Features and Benefits
Promotional Story
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References

INDICATIONS

The Simpulse™VariCare™ Suction/Irrigator is designed to provide controlled powered irrigation during general surgical procedures and for the cleansing and debridement of burns or wounds. The pulsatile action of the pump helps to remove blood, tissue debris and foreign matter from the operative or wound site. When connected to a suction source, the device aspirates fluids and debris from the operative or wound site.

WARNINGS:

  1. Do not resterilize.
  2. This device has been designed for single use only. Reuse, reprocessing, resterilization or repackaging may compromise the structural integrity and/or essential material and design characteristics that are critical to the overall performance of the device and may lead to device failure which may result in injury to the patient. Reuse, reprocessing, resterilization or repackaging may also create a risk of contamination of the device and/or cause patient infection or cross infection, including, but not limited to, the transmission of infectious diseases from one patient to another. Contamination of the device may lead to injury, illness or death of the patient or end user.
  3. Do not use in an oxygen-enriched atmosphere due to explosion hazard.
  4. Do not incinerate the batteries as this can cause a risk to the environment.
  5. Do not recharge batteries, put in backwards, or mix with used or other battery types as these actions may cause explosion or leakage leading to personal injury or can cause a risk to the environment.
  6. After use, this product may be a potential biohazard. Handle and dispose of in accordance with accepted medical practice and applicable local, state and federal regulations.
  7. Follow Occupational Safety and Health Administration (OSHA) standards or Universal Precautions for bloodborne pathogens (29 CFR-1910.1030). These may be found by searching the OSHA web site at www.osha.gov.
  8. In order to limit contact with infectious agents from mist and splashing, personnel using or patient exposed to the Simpulse™VariCare™ Suction/Irrigator must wear personal protective equipment.
  9. To prevent possible exposure of other patients to aerosol, the patient should be treated in a private area, enclosed with walls and doors, separate from other patients.
  10. Use continuous suction at 60-100 mmHg to keep operative or wound site clean.
  11. Keep splash shield in contact with wound/periwound at all times to prevent aerosolization.
  12. VariCare™ is approved as a Class A device per IEC 60601-1-2 for use in a hospital or health care setting. Testing for use in other environments (i.e. home use) has not been performed and may affect the operation of other devices in the same environment.

PRECAUTIONS:

  • Single use.
  • If package is damaged or open, do not use product.
  • Read all instructions prior to use.
  • Do not submerge handle in liquid as this may compromise efficiency of the pump or alter the pH of the liquid.
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Specification

GTIN - Box

10801741065313

5

GTIN - each

00801741065316

1

GTIN - Case

20801741065310

10


Quantity

10/cs.


Dimensions

Simpulse™ VariCare™ Wound Management Kit with VariCare™ Small Retractable Splash Shield (1.25" diameter) Wound Tip, Cojoined Suction and Irrigation Tubing, Dual Spike Adapter, and SprayGuard™ Sheet

GTIN

GTIN - Box 10801741065313 5
GTIN - each 00801741065316 1
GTIN - Case 20801741065310 10

Packaging

Quantity 10/cs.

Product Basic Specification

Dimensions Simpulse™ VariCare™ Wound Management Kit with VariCare™ Small Retractable Splash Shield (1.25" diameter) Wound Tip, Cojoined Suction and Irrigation Tubing, Dual Spike Adapter, and SprayGuard™ Sheet
References
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Electronic Instructions for Use (eIFUs)
Resources
References
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Frequently Asked Questions
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Related Products
RELATED PRODUCTS NOT AVAILABLE
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Product Complaints
North American Regional Complaint Center
1-844-8BD-LIFE (1-844-823-5433)
Things to Consider

If you are a patient or end user, you can contact us yourself, or you may have your caregiver or your physician do that for you. To help us process your
information quickly and effectively, please contact our customer complaints
team.

To better facilitate our investigation, please include the following information in your reporting:


  • Product Name and/or Catalog Number
  • Lot Number or Serial Number
  • Any injuries and/or Harm?
  • What is the issue you experienced?
  • Is the actual sample or sample representative available? (If possible, please send affected sample)
  • Contact name and phone number
Product Recalls
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Recall Notifications
These recall notices provide current information on medical device recalls.
Learn more
References
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