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3M™ V.A.C.® Simplicity Therapy System

The 3M™ V.A.C.® Simplicity Therapy System is an NPWT system that automatically delivers the most commonly prescribed therapy (continuous -125mmHg).

3M Health Care

3M focuses on providing better care through patient-centered science. From wound and skin care to solutions for BSI and SSI risk reduction, 3M is ready to partner with health care providers to help transform outcomes.
Toll free:(800) 228-3957 Fax:(800) 728-0959 Website: www.3m.com/medical
Benefits

• Easy to use
• Features SENSAT.R.A.C.™ Technology, a real-time pressure feedback system that adjusts pump output, compensating for wound distance, wound position, exudate characteristics, and patient movement
• Simple user interface minimizes device training time
• Quick release canisters
• Multi-orientational canister allows for patient mobility and product position flexibility
• 300ml canister minimizes canister changes
• Long battery life (8+ hours) with fast recharge time (6 hours)
• Lightweight and portable

Indications

The 3M™ V.A.C.® Simplicity Therapy System is an integrated wound management system for use in acute, extended, and home care settings. It is intended to create an environment that promotes wound healing by secondary or tertiary (delayed primary) intention by preparing the wound bed for closure, reducing edema, promoting granulation tissue formation and perfusion and by removing exudate and infectious material. It is indicated for patients with chronic, acute, traumatic, subacute and dehisced wounds, partial-thickness burns, ulcers (such as diabetic or pressure), flaps, and grafts.

When used on closed surgical incisions, it is intended to manage the environment of surgical incisions that continue to drain following sutured or staple closure by maintaining a closed environment and removing exudates via the application of negative pressure wound therapy.

Contraindications

Do not place foam dressings of the V.A.C.® Therapy System directly in contact with exposed blood vessels, anastomotic sites, organs, or nerves.
NOTE: Refer to Warnings section for additional information concerning bleeding or osteomyelitis.
• V.A.C.® Therapy is contraindicated for patients with:
• Malignancy in the wound
• Untreated osteomyelitis
• Non-enteric and unexplored fistulas
• Necrotic tissue with eschar present
• Sensitivity to silver (V.A.C.® Granufoam™ Silver Dressing only)
NOTE: After debridement of necrotic tissue and complete removal of eschar, V.A.C.® Therapy may be used.

Warnings and Precautions

Bleeding: With or without using V.A.C.® Therapy, certain patients are at high risk of bleeding complications. The following types of patients are at increased risk of bleeding, which, if uncontrolled, could be potentially fatal.
• Patients who have weakened or friable blood vessels or organs in or around the wound as a result of, but not limited to:
• Suturing of the blood vessel (native anastamoses or grafts)/organ
• Infection
• Trauma
• Radiation
• Patients without adequate wound hemostasis
• Patients who have been administered anticoagulants or platelet aggregation inhibitors
• Patients who do not have adequate tissue coverage over vascular structures.
If V.A.C.® Therapy is prescribed for patients who have an increased risk of bleeding complications, they should be treated and monitored in a care setting deemed appropriate by the treating physician.
If active bleeding develops suddenly or in large amounts during V.A.C.® Therapy, or if frank (bright red) blood is seen in the tubing or in the canister, immediately stop V.A.C.® Therapy, leave dressing in place, take measures to stop the bleeding, and seek immediate medical assistance.
The V.A.C.® Therapy Units and dressings should not be used to prevent, minimize or stop vascular bleeding.
• Protect Vessels and Organs: All exposed or superficial vessels and organs in or around the wound must be completely covered and protected prior to the administration of V.A.C.® Therapy.
Always ensure that V.A.C.® Foam Dressings do not come in direct contact with vessels or organs. Use of a thick layer of natural tissue should provide the most effective protection. If a thick layer of natural tissue is not available or is not surgically possible, multiple layers of fine-meshed, non-adherent material, or bio-engineered tissue may be considered as an alternative, if deemed by the treating physician to provide a complete protective barrier. If using non-adherent materials, ensure that they are secured in a manner as to maintain their protective position throughout therapy.
Consideration should also be given to the negative pressure setting and therapy mode used when initiating therapy.
Caution should be taken when treating large wounds that may contain hidden vessels, which may not be readily apparent. The patient should be closely monitored for bleeding in a care setting deemed appropriate by the treating physician.
• Infected Blood Vessels: Infection may erode blood vessels and weaken the vascular wall which may increase susceptibility to vessel damage through abrasion or manipulation. Infected blood vessels are at risk of complications, including bleeding, which, if uncontrolled, could be potentially fatal. Extreme caution should be used when V.A.C.® Therapy is applied in close proximity to infected or potentially infected blood vessels. (Refer to Protect Vessels and Organs section above.)
• Hemostasis, Anticoagulants, and Platelet Aggregation Inhibitors: Patients without adequate wound hemostasis have an increased risk of bleeding, which, if uncontrolled, could be potentially fatal. These patients should be treated and monitored in a care setting deemed appropriate by the treating physician. Caution should be used in treating patients on doses of anticoagulants or platelet aggregation inhibitors thought to increase their risk for bleeding (relative to the type and complexity of the wound). Consideration should be given to the negative pressure setting and therapy mode used when initiating therapy.
• Hemostatic Agents Applied at the Wound Site: Non-sutured hemostatic agents (for example, bone wax, absorbable gelatin sponge, or spray wound sealant) may, if disrupted, increase the risk of bleeding, which, if uncontrolled, could be potentially fatal. Protect against dislodging such agents. Consideration should be given to the negative pressure setting and therapy mode used when initiating therapy.
• Sharp Edges: Bone fragments or sharp edges could puncture protective barriers, vessels, or organs causing injury. Any injury could cause bleeding, which, if uncontrolled, could be potentially fatal. Beware of possible shifting in the relative position of tissues, vessels or organs within the wound that might increase the possibility of contact with sharp edges. Sharp edges or bone fragments must be eliminated from the wound area or covered to prevent them from puncturing blood vessels or organs before the application of V.A.C.® Therapy. Where possible, completely smooth and cover any residual edges to decrease the risk of serious or fatal injury, should shifting of structures occur. Use caution when removing dressing components from the wound so that wound tissue is not damaged by unprotected sharp edges.
1000ml Canister: DO NOT USE the 1000ml canister on patients with a high risk of bleeding or on patients unable to tolerate a large loss of fluid volume, including children and the elderly. Consider the size and weight of the patient, patient condition, wound type, monitoring capability and care setting when using this canister. This canister is recommend for acute care (hospital) use only.

Storage Requirements

Storage Conditions:
Storage Temperature Range: -20°C-60°C
Relative Humidity Range: 0% to 95% non-condensing

Operating Conditions:
Operational Temperature Range: 5°C-40°C
Relative Humidity Range: 0% to 95% non-condensing

HCPCS Code
Product features
check_circle Accommodates large wounds
check_circle Accommodates small wounds
cancel Adjustable PSI
check_circle Antimicrobial interface available
check_circle Battery-operated
cancel Disposable
check_circle Foam interface
cancel Gauze interface
cancel Instillation function
cancel Intermittent-pressure setting
cancel Irrigation function
cancel Portable (under 1lb)
cancel Single-use – 10 days
cancel Single-use – 15 days
cancel Single-use – 30 days
cancel Single-use – 7 days
cancel Touchscreen
check_circle Usable on closed wounds
check_circle Usable on open wounds
cancel Variable pressure setting
Other features
check_circle Educational Material Available
check_circle Free Samples/Trials Available
check_circle Published Clinical Article Available
Recommended Use

Acute Wounds
Chronic Wounds
Deep Wounds
Dehisced Wounds
Diabetic Ulcers
Flaps and Grafts
Granulating Wounds
Moderate/Highly Exudating Wounds
Non/Minimally Exudating Wounds
Partial-Thickness Burns
Pressure Ulcers
Skin Flaps
Skin Grafts
Subacute Wounds
Surgical Wounds
Traumatic Wounds
Venous Ulcers

Clinically Tested

Latex-friendly

Technical Specifications

Dimensions: 7.6"x6"x6.4"
Weight: 2.3lb
Canister volume: 300ml
Battery Life: 8+ hours
Recharge time: <six hours

Electrical Data:
Electrical Charger/External Supply Input: 100-240V AC .72A @ 115V AC 50/60Hz
Charger/External Supply Output: 12V, 3.3A
Maximum Electrical Leakage: <100 Microamps

Therapy Options:
Negative Pressure: -125mmHg
Mode of Operation: Continuous
Intensity: High

IEC Classification:
Type B Applied Part, Class II, IPX0

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