Prevena Plus Duo Peel and Place Incision Management System

The Prevena™ Plus Duo Peel and Place Incision Management System is an advanced dual-incision NPWT (negative pressure wound therapy) device designed to support complex surgical cases with two incision sites. Ideal for hospital, outpatient, and home recovery settings, the system optimizes healing by reducing edema, securing wound edges, and protecting incisions from external contamination.

Overview

The Prevena™ Plus Duo delivers continuous −125 mmHg negative pressure for up to 7 days through two integrated Peel and Place dressings connected to a single, compact therapy unit. Its integrated foam dressing evenly distributes pressure, channels fluid into a 45 mL canister, and includes built-in alerts for leaks, battery status, and canister fill level. The portable device supports patient mobility and is waterproof—allowing showering while maintaining therapy.

Key Features

• Dual-incision coverage: Delivers negative pressure to two adjacent incision sites with one therapy unit.
• Continuous −125 mmHg NPWT: Promotes tissue approximation, reduces swelling, and supports faster healing.
• Preassembled dressings: Peel and Place design enables quick application with minimal training.
• Integrated foam reservoir: Ensures even pressure distribution and efficient exudate management.
• Portable, battery-powered unit: Lightweight (~0.4 lb) and mobile, supporting patient comfort and early ambulation.
• 45 mL canister: Single-use fluid collection with secure, easy disposal.
• Smart alerts: Visual and audible notifications for device integrity, power, and canister status.
• Waterproof design: Allows patients to shower without interrupting therapy.

Product Specifications

• Dressing layout: Dual Peel and Place dressings in various combined lengths (example: 2 × 10 cm)
• Therapy unit weight: Approximately 0.4 lb (0.2 kg)
• Unit dimensions: Approximately 13.6 cm × 7.5 cm × 3 cm
• Canister capacity: 45 mL fluid collection
• Battery: Pre-installed 3 × AA batteries (up to 7-day runtime)
• Operating temperature: 5–40 °C (41–104 °F); storage: –20–60 °C (–4–140 °F)
• Materials: Latex-free, non-cytotoxic; dressing width 1.8 cm
• Duration of therapy: Up to 7 continuous days per dressing application
• Regulatory compliance: Classified as Class II medical device (FDA-cleared)

Ideal For

• Hospital post-operative recovery with bilateral or multiple incision sites
• Outpatient surgical centers using enhanced recovery protocols
• Home-care environments needing extended NPWT support
• Orthopedic, cardiac, abdominal, plastic, and vascular surgery patients with two incisions
• Wound care clinics focused on reducing surgical site complications