Muscle tightness melts away in the warming comfort of the VivaLift!® Radiance Power Recliner. The Radiance Collection is the first in its class to offer three heating pads, and with the VivaLift!® true infinite positioning, you can take your relaxation experience to the next level.
| CATEGORY |
SPECIFICATION |
| Model |
VivaLift!® Radiance - PLR-3955PW
|
| Position |
True-Infinite Chaise Lounger |
| Size |
Petite Wide |
| Height Range |
5'4" and below |
| Weight Capacity |
400 lbs. |
| Seat to Floor |
19.5" |
| Seat Depth |
18" |
| Seat Width |
24" |
| Top of Back to Seat |
23" |
| Footrest Extension |
Standard |
| Back Style |
Deluxe Biscuit Back |
| Fully Padded Chaise |
Yes |
| Additional Option(s) |
No |
| Seating Type |
Total Comfort |
| Chair Height |
40" |
| Distance From Wall |
14" |
| Overall Chair Width |
41" |
| Chair Weight |
161 lbs. |
| Warranty |
7- Year Prorated |
| Fabric Options |
Silt
Walnut
Ocean
Steel |
|
The information contained herein is correct at the time of publication; we reserve the right to alter specifications without prior notice.
Warranty
FDA Class II Medical Device*
Meeting and Exceeding High Standards for your Peace of Mind.
Your Pride product has undergone thorough product testing to ensure safety, durability and performance.
Our power chairs, scooters and lift chairs are FDA medical devices that require specific testing prior to release for public use.
The testing requirements accepted by the FDA were developed by the American National Standards Institute/Rehabilitation Engineering & Assistive Technology Society of North America (ANSI/RESNA).
The tests are conducted in accordance with the requirements of the ANSI/RESNA Test Standards and complement an additional stringent testing regimen developed by Pride's Research & Development Team.
All products have passed, and in many cases, exceeded test criteria set forth, assuring the high level of quality synonymous with Pride.
In addition to “real world” testing developed by Pride during more than thirty years of designing Lift Chairs, our products are subjected to a host of standardized testing criteria, including but not limited to:
- ANSI/AAMI/ES60601-1, Medical Electrical Equipment--Part 1: General Requirements for Basic Safety and Essential Performance, and ANSI/AAMI/IEC 60601-1-2, Medical Electrical Equipment--Part 1-2: General Requirements for Basic Safety and Essential Performance--Collateral Standard: Electromagnetic Disturbances--Requirements and Tests
- ANSI/AAMI/ISO 10993-5, Biological Evaluation of Medical Devices--Part 5: Tests for In Vitro Cytotoxicity, and ANSI/AAMI/ISO 10993-10, Biological Evaluation of Medical Devices--Part 10: Tests for Irritation and Skin Sensitization
- IEC 62304, Medical Device Software--Software Life Cycle Processes
- IEC 60335-1:2012, Safety of Household Electrical Appliances
- ISO 14971 Medical devices – Application of risk management to medical devices
- EN 12182, Assistive products for persons with disability. General requirements and test methods
- Static Load and Stability Tests
- Strength & Fatigue Verification Tests
- Overall Product Performance Verification
- Dimensional Requirement Compliance
- Armrest Force Test
- Material Protective Coating Testing Verification
- Misuse and Abuse Testing
- Ergonomic Verification
- Environmental Testing for Adverse Conditions
- Electronic Systems Performance and Durability
- Chemical and Bio-Contamination Analysis Testing for Toxicity Verification
- Cal 117 Flammability Test Compliance for Seating Foam and Fabric Components
- UL94VO Flammability Testing for Compliance of Plastic Components
- Electromagnetic Compatibility (EMC)
Warranty
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