Lymphatic Arm Sleeve, Pressure Bandage, Elbow Wrist Support, Postoperative Swelling Relief, Waterproof Fixation

Comprehensive Lymphatic Support and Postoperative Recovery Sleeve

Product Overview

The Lymphatic Arm Sleeve with Integrated Elbow-Wrist Support is a clinically designed pressure bandage system engineered to address postoperative swelling and enhance recovery for individuals undergoing breast cancer treatment. Combining targeted compression, joint stabilization, and waterproof functionality, this medical-grade sleeve provides holistic support during critical phases of rehabilitation.

Indications and Target Patient Groups

This device is specifically indicated for:

• Patients recovering from axillary lymph node dissection (ALND) surgery
• Individuals undergoing adjuvant radiotherapy or chemotherapy for breast cancer
• of early-stage postoperative lymphedema and localized swelling
• Prevention of secondary complications in high-risk mobility-limited patients

Key Functional Advantages

1. Dynamic Compression Technology

• Graduated pressure gradient (20-30 mmHg) facilitates lymphatic drainage
• Reduces interstitial fluid accumulation in forearm and upper arm regions
• Clinically validated for swelling reduction (average 34% volume decrease in Week 1 trials)

2. Integrated Orthopedic Support

• Anatomic elbow stabilization cup prevents hyperextension
• Wrist compression cuff maintains neutral positioning
• Dual-joint protection during activities of daily living (ADLs)

3. Advanced Material Properties

layer

• Hypoallergenic, latex-free construction (ISO 10993-10 certified)
• Breathable 3D-knit technology prevents maceration

4. Waterproof Fixation System

• Silicone grip bands maintain positional integrity during hydrotherapy
• Seamless integration with post-op wound dressings
• Sterilisable surface for infection control compliance

Clinical Application Protocol

For optimal therapeutic outcomes:

• Phase 1 (0-2 weeks post-op): 23-hour daily wear with physician-supervised donning
• Phase 2 (3-6 weeks): 12-hour daytime wear during active mobilization
• Maintenance: Night wear during radiotherapy cycles

Note: This device requires prescription and fitting by certified lymphedema therapists. Not intended for Stage III lymphedema or venous thrombosis.

Comprehensive Lymphatic Support and Postoperative Recovery Sleeve

Product Overview

The Lymphatic Arm Sleeve with Integrated Elbow-Wrist Support is a clinically designed pressure bandage system engineered to address postoperative swelling and enhance recovery for individuals undergoing breast cancer treatment. Combining targeted compression, joint stabilization, and waterproof functionality, this medical-grade sleeve provides holistic support during critical phases of rehabilitation.

Indications and Target Patient Groups

This device is specifically indicated for:

• Patients recovering from axillary lymph node dissection (ALND) surgery
• Individuals undergoing adjuvant radiotherapy or chemotherapy for breast cancer
• of early-stage postoperative lymphedema and localized swelling
• Prevention of secondary complications in high-risk mobility-limited patients

Key Functional Advantages

1. Dynamic Compression Technology

• Graduated pressure gradient (20-30 mmHg) facilitates lymphatic drainage
• Reduces interstitial fluid accumulation in forearm and upper arm regions
• Clinically validated for swelling reduction (average 34% volume decrease in Week 1 trials)

2. Integrated Orthopedic Support

• Anatomic elbow stabilization cup prevents hyperextension
• Wrist compression cuff maintains neutral positioning
• Dual-joint protection during activities of daily living (ADLs)

3. Advanced Material Properties

layer

• Hypoallergenic, latex-free construction (ISO 10993-10 certified)
• Breathable 3D-knit technology prevents maceration

4. Waterproof Fixation System

• Silicone grip bands maintain positional integrity during hydrotherapy
• Seamless integration with post-op wound dressings
• Sterilisable surface for infection control compliance

Clinical Application Protocol

For optimal therapeutic outcomes:

• Phase 1 (0-2 weeks post-op): 23-hour daily wear with physician-supervised donning
• Phase 2 (3-6 weeks): 12-hour daytime wear during active mobilization
• Maintenance: Night wear during radiotherapy cycles