Summary & Overview
HCPCS E2364: Power Wheelchair U-1 Non-Sealed Lead Acid Battery, Each
HCPCS Level II code E2364 designates a U-1 non-sealed lead acid battery sold as a single accessory for power wheelchairs. This supply-level code matters nationally because batteries are essential to power mobility device function and recurring replacement creates ongoing cost and coverage considerations for payers, suppliers, and patients. Coverage, billing practices, and allowed amounts for replacement batteries can influence access to mobility and out-of-pocket spending.
Key payers discussed include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find an overview of the code’s clinical and supply context, common billing pathways, and typical sites where the item is furnished. The publication also outlines benchmarks for billing and reimbursement where available, summarizes relevant policy updates affecting DME battery replacement, and highlights operational considerations for suppliers and billing staff. Data regarding modifiers, associated taxonomies, specific ICD-10 pairing, and related codes is not available in the input. The report is intended for a national audience of payers, DME suppliers, case managers, and policy analysts seeking concise guidance on coding and coverage considerations for power wheelchair batteries.
Billing Code Overview
HCPCS Level II code E2364 describes a power wheelchair accessory: U-1 non-sealed lead acid battery, each. This item is a replacement or spare battery intended for use with a power wheelchair and is billed per battery.
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Service type: Durable medical equipment accessory (power mobility supply)
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Typical site of service: Durable medical equipment supply channels, home delivery, or outpatient durable medical equipment (DME) suppliers
Clinical & Coding Specifications
Clinical Context
A patient with a mobility impairment presents to a durable medical equipment (DME) supplier or mobility clinic for replacement batteries for a power wheelchair. Typical patients include those with spinal cord injury, multiple sclerosis, cerebral palsy, severe osteoarthritis, or other neuromuscular disorders who rely on a power wheelchair for community mobility. The clinical workflow: the clinician or DME specialist documents medical necessity in the patient record, including diagnosis, functional limitations, and mileage/use needs; verifies the wheelchair model and battery type; checks warranty and prior replacements; obtains any required prior authorization from the payor; orders the E2364 item (power wheelchair accessory, U-1 non-sealed lead acid battery, each); schedules delivery and installation or instructs the patient on safe battery replacement and disposal. Billing is submitted to the patient’s primary payor with applicable modifier(s) to indicate professional/technical components, rentals, or bilateral/multiple items as appropriate. Patient education on charging, safe handling, and maintenance is provided at delivery.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
00 | No modifier / default | Use when no special modifier applies to the supply claim. |