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Solventum
PRE1101US - Solventum 3M™ Prevena™ Incision Management - Peel & Place™ System Kit, 15.2 cm, 7 Day Pump, 5 kits/cs
PRE1101US - Solventum 3M™ Prevena™ Incision Management - Peel & Place™ System Kit, 15.2 cm, 7 Day Pump, 5 kits/cs
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3M™ Prevena™ Incision Management - Peel & Place™ System Kit, 15.2 cm, 7 Day Pump, 5 kits/cs
Please note: All prices are for cases.
The Solventum 3M™ Prevena™ Peel & Place™ System (SKU PRE1101US) is a disposable negative pressure wound therapy (NPWT) system specifically designed for the management of closed surgical incisions. This kit includes a 15.2 cm (approx. 6 inch) integrated one-piece dressing and a dedicated 7-day single-use pump. The system delivers a continuous negative pressure of -125 mmHg, which helps to hold incision edges together, reduce lateral tension, and remove fluid and infectious materials into a replaceable canister.
Key Features
- Integrated Peel & Place™ Dressing: A one-piece, foam-based dressing designed for easy, wrinkle-free application on linear incisions up to 13 cm in length.
- Continuous Negative Pressure: Delivers a constant -125 mmHg to the incision site for up to 7 days to stabilize the wound environment and reduce edema.
- Silver-Infused Interface Layer: The skin contact layer contains 0.019% ionic silver, which helps reduce bacterial colonization within the dressing fabric.
- Replaceable 45ml Canister: Collects and stores exudate away from the incision site; the system includes audible and visual alerts for "canister full" or "leak" conditions.
- Portable 7-Day Therapy Unit: A lightweight, battery-operated pump (powered by 3 AA batteries) designed for single-patient use over a 192-hour lifespan.
- Shower-Friendly Design: The dressing is water-resistant, allowing for light showering while the therapy unit is disconnected and the tubing is capped.
Ideal Clinical Applications
- Orthopedic Procedures: Large-joint replacements (hip/knee) where reducing seroma and tension is critical.
- Plastic and Reconstructive Surgery: Protection of primary closures in abdominoplasty or breast reconstruction.
- General and Vascular Surgery: Management of high-risk incisions in patients prone to surgical site complications (SSIs).
- Cardiac and Thoracic Surgery: Stabilization of sternotomy incisions or long linear closures.
Product Details
Brand: Prevena™ Peel & Place™ (Solventum)
Product Type: Single-Use Closed Incision Negative Pressure Therapy (ciNPT)
Compatible With: Prevena™ Patch Strip Dressings (for sealing reinforcement)
Latex Status: Not Made with Natural Rubber Latex
Single-Use / Reusable: Single-Use
Packaging
3M™ Prevena™ Incision Management - Peel & Place™ System Kit, 15.2 cm, 7 Day Pump, 5 kits/cs
Kit Content: (1) Prevena™ 125 Therapy Unit, (1) Prevena™ Peel & Place™ Dressing, (1) Prevena™ 45ml canister, (1) Prevena™ Carrying Case, (1) Set of Prevena™ Patch Strips, (1) V.A.C® Therapy Unit Connector, (1) Rule w/ Sticker
5 kts/cs
Safety Data Sheet (SDS)
To view the manufacturer's most current and up-to-date safety information, please click here.
Important Safety Information
MRI Unsafe: The Prevena™ 125 Therapy Unit is MRI Unsafe. The pump must be disconnected and removed from the MRI environment.
Hyperbaric Oxygen (HBO) Contraindication: Do not take the therapy unit or dressing into a hyperbaric oxygen chamber; it is not designed for this environment and is considered a fire hazard.
Hemostasis Requirement: Adequate hemostasis must be achieved before application. If active bleeding, frank blood in the tubing, or a sudden large amount of blood is observed, the unit must be turned off and immediate medical assistance sought.
Defibrillation Warning: The dressing must be removed if defibrillation is required in the area of placement to ensure proper energy transmission.
Allergic Sensitivity: Do not use on patients with a known allergy or hypersensitivity to acrylic adhesives or silver.
Circulatory Compromise: Do not apply the dressing circumferentially. Monitor distal pulses and circulatory status; discontinue use if compromise is suspected.
Pediatric Population: Safety and effectiveness have not been evaluated in patients under 22 years of age.
Wound Class Limitation: Indicated for Class I and Class II (clean/clean-contaminated) closed incisions only; not demonstrated for use on Class III (contaminated) or Class IV (dirty/infected) wounds.
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