(Classified FDA Class II Medical Device)
| CATEGORY | SPECIFICATION |
|---|---|
| Model1 | Go Go® Carbon |
| Model Number | SC25M |
| Weight Capacity | 300 lbs. |
| Turning Radius | 53" |
| Overall Width3 | 17.5" |
| Overall Length3 | 40.3" |
| Maximum Speed2 | Up to 3.7 mph |
| Ground Clearance3 | 1.5"at motor |
| Front Wheels | 7" solid |
| Rear Tires | 8" solid |
| Number of Tires | 4 |
| Drivetrain | Rear wheel drive, sealed transaxle, 24-volt brushless |
| Braking System | Regenerative and electromechanical |
| Suspension Type | NA |
| Seat Sizes | 14"W x 11.5"D |
| Seat-to-Floor-Range | 21.75" |
| Per Charge Range13,5 | Up to 10 miles |
| Standard Electronics | 30A Brushless controller |
| Component Weights6 | 35 lbs. without battery With battery: 39 lbs. |
| Battery Requirements4 | 24V, 12Ah lithium battery |
| Battery Charger | 24V, 2A |
| Warranty | Frame: lifetime limited; Drivetrain: 1-year; Electronics: 1-year; Battery: 1-year |
| Notes: 1 1This product is a FDA Class II Medical Device designed to aid individuals with mobility impairments. 2 Varies with user weight, terrain type, battery amp-hour (AH), battery charge, battery condition and tire condition. These specifications can be subject to a variance of (+/- 10%). 3 Due to manufacturing tolerances and continual product improvement, this specification can be subject to a variance of (+ or - 3%). 4 AGM or gel cell type required. 5 Tested in accordance with ANSI/RESNA, WC Vol2, section 4 & ISO 7176-4 standards. Results derived from theoreticl calculations based on battery specifications and drive system performance. Test conducted at maximum weight capacity. 6 Battery weight may vary based on manufacturer. | |
| The information contained herein is correct at the time of publication; we reserve the right to alter specifications without prior notice. |
Go Go® Carbon
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 Food & Drug Administration (FDA) approved medical products 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 regiment 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.
Some of the items our testing criteria include are:
- Product Stability & Brakes Effectiveness Tests
- Fatigue & Impact Strength Verification Tests
- Overall Product Performance Verification
- Dimensional Requirement Compliance
- Product Durability & Reliability Testing
- Material Protective Coating Testing Verification
- Misuse and Abuse Testing
- Ergonomic Verification
- Environmental Testing for Adverse Weather Operation 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
- Frame: lifetime limited
- Drivetrain: 1-year
- Electronics: 1-year
- Battery: 1-year