OEM / ODM PRODUCT SOURCING
Electric mobility platforms
for OEM/ODM sourcing.
Compare electric wheelchairs and mobility scooters by buyer search intent, frame, battery and model-specific documentation before quotation.
PRODUCT SCOPEElectric wheelchairs
Mobility scooters
PROCUREMENT COMPARISON
Compare the fields
that change sourcing cost.
Numeric specifications are issued only after the model and configuration are confirmed. This keeps pricing, logistics and market documentation traceable to the exact product.
On smaller screens, scroll horizontally to review both product lines.
Product platform comparison framework
| Procurement field | Electric wheelchair | Mobility scooter |
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| Buyer search path | Lightweight folding / Standard / Heavy-duty | Portable / Classic / Heavy-duty |
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| Battery options | Lithium / Lead-acid | Confirmed per selected model |
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| Frame material options | Carbon fiber / Magnesium / Aluminum / Carbon steel | Magnesium / Aluminum / Iron |
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| FDA 510(k) record scope | K232121: BC-EA8000
K250475: BC-EA5516 / BC-EC8002 / BC-EC8003 / BC-EALD3 | K252817: BC-MS310 |
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| Model specification pack | Dimensions, net and gross weight, load, battery, range and packaging — confirmed per model | Dimensions, net and gross weight, load, battery, range and packaging — confirmed per model |
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| Battery freight planning | Lithium or lead-acid battery options; shipment route and required documents reviewed for the selected model | Battery type, shipment route and required documents reviewed for the selected model |
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| Commercial quotation | MOQ, sample timing, production timing and container loading — confirmed per project | MOQ, sample timing, production timing and container loading — confirmed per project |
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MODEL-SPECIFIC RECORDS
Compliance evidence,
separated by product line.
No record on this page is presented as applying to every model. Confirm the target model and market before labeling or import planning.
ELECTRIC WHEELCHAIRFDA product code ITI
- FDA 510(k) cleared — K232121 (Power Wheelchair, Model BC-EA8000)
- FDA 510(k) cleared — K250475 (Electric Wheelchair, BC-EA5516 / BC-EC8002 / BC-EC8003 / BC-EALD3)
- CE Marked under EU MDR 2017/745
- EU Authorised Representative: NL-AR-000000247
- Basic UDI-DI: 697518562ewheelchair001YK (Wheelchair)
MOBILITY SCOOTERFDA product code INI
- FDA 510(k) cleared — K252817 (Mobility Scooter, Model BC-MS310)
- CE Marked under EU MDR 2017/745
- EU Authorised Representative: NL-AR-000000247
- Basic UDI-DI: 697518562BCMS001QU (Mobility Scooter)
QUALITY MANAGEMENTISO 13485 certified (Cert. No. 133093, issued by NQA, valid until 2026-10-18)
POWERED WHEELCHAIR BATTERY-SYSTEM REPORTTested to ISO 7176-31:2023 (Li-ion battery systems & chargers), Report No. SGTHF-202503001-01
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Medical mobility
