Non-Woven Swallowing Electrode Pads with 2.0mm Female Pin Interface
These self-adhesive non-woven electrode pads are designed as a skin-contact interface for compatible NMES, TENS and swallowing rehabilitation equipment. Each electrode assembly uses two separate 2.0mm female pin connections, allowing the pad to connect with compatible stimulation lead wires while maintaining a compact and flexible electrode structure.
Electrode shape, dimensions, backing material, adhesive configuration, connector structure, labeling and packaging can be developed according to OEM/ODM project requirements. Final electrode placement, electrical parameters and operating method should follow the approved specification and instructions of the completed device.
Flexible Non-Woven Electrode Structure for Neck and Throat Placement
The electrode uses a flexible non-woven backing that allows the pad to conform to the intended skin-contact area. The elongated shape is designed around compatible neck and throat electrode-placement configurations while keeping the lead-wire connections positioned away from the main contact area.
Electrode dimensions and geometry should be selected according to the target equipment and intended product design. Placement should not be determined from the electrode shape alone and should follow the finished-device instructions and validated application method.
For OEM projects, the overall outline, conductive area, connector exit position and backing structure can be adjusted to better match the equipment and accessory system.
Dual 2.0mm Female Pin Connections for Detachable Lead Wires
The electrode assembly uses two 2.0mm female pin interfaces, allowing the pad to connect with compatible male electrode lead wires. This detachable structure makes it possible to replace the electrode pad separately from the reusable device cable.
Nominal connector diameter alone does not guarantee compatibility. Pin diameter, insertion depth, mating geometry, polarity and electrical configuration should be checked against the actual lead wire before sampling or production.
For equipment requiring a matching 1-to-2 cable architecture, our DC 2.35mm to Dual 2.0mm Electrode Lead Wire provides one example of a compatible-style 2.0mm electrode connection structure.
Electrode Pad and Lead Wire Should Be Evaluated as One Connection System
A skin-contact electrode pad should not be selected independently from the stimulation cable and target equipment. Electrode geometry, connector interface, lead-wire structure, electrical output and intended placement all influence the final system configuration.
Heymed Medical can review the electrode pad and matching cable together during product development. Customers can provide equipment models, cable drawings, connector dimensions, electrical definitions or existing samples before prototype production.
Additional lead wires, electrode pads and related accessories can be reviewed through our TENS & EMS Cables & Electrode Accessories range according to the target equipment.
Key Customization Options
Electrode geometry: Overall length, width, shape and contact-area layout can be developed according to project requirements.
Backing material: Non-woven structure and flexibility can be selected according to the intended product design.
Adhesive configuration: Adhesion characteristics and skin-contact construction can be reviewed according to the finished product requirements.
Connector interface: 2.0mm female pin structure, cable exit position and project-specific connector configurations can be evaluated.
Product identification: Labeling, markings and customer-specific product information can be customized.
Packaging: Individual pouch, pack quantity, private-label artwork and outer packaging can be developed for OEM/ODM programs.
Skin-Contact Materials and Product Requirements
Because the electrode is intended for direct skin contact, material selection should be reviewed as part of the completed product rather than based only on the visible backing material. Adhesive system, conductive structure, wear duration, storage conditions and shelf-life requirements should be defined according to the target product and market.
Where biocompatibility, labeling or other compliance requirements apply, the required verification should be established according to the finished product classification and applicable regulatory pathway.
For projects requiring customized electrode pads together with matching cables or connectors, development can also be supported through our Custom Medical Cable Assemblies engineering capability.
From Electrode Sample to OEM/ODM Production
Custom swallowing electrode development can begin from an existing electrode sample, dimensional drawing, target equipment interface or complete accessory specification. Our engineering team can review the electrode shape, connector structure, backing material and matching lead-wire requirements before preparing samples.
During prototype evaluation, electrode dimensions, connector fit, cable continuity, adhesive construction and overall assembly can be checked against the approved project requirements.
Once the configuration is confirmed, electrode converting, connector assembly, inspection, labeling and packaging can be transferred into repeatable OEM/ODM production according to the approved specification.
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