Reusable purple lancing device for professional diabetes-testing supply programs. Review the ELD-1 product reference, ELD-2.0 inside code, adjustable depth configuration, compatible BL-30G / BL-30E lancet entry, operating features, packaging and available documentation before ordering.
Current published product reference
Current listed internal code
Compatibility must be confirmed by SKU
Current published device pack
Use the exact device reference and compatible-lancet reference in quotations and purchase orders. Depth-setting details, operating configuration, labeling, packaging and documentation should be verified against the selected SKU rather than inferred from a similar lancing device.
Current website information is shown below. Final compatibility, labeling, IFU, pack configuration and available records should be confirmed during product review.
| Description | REF | Inside Code | Qty / Box | Qty / Case | Procurement Control |
|---|---|---|---|---|---|
| Purple Lancing Device | ELD-1 | ELD-2.0 | 1 pc | 20 pcs | Confirm exact device configuration and IFU |
| Compatible Lancet Entry | BL-30G | BL-30E | 100 pcs | 10,000 pcs | Confirm compatibility with the quoted ELD-1 configuration |
Confirm the ELD-1 device together with the intended lancet REF, lancet dimensions, loading interface, removal method and current compatibility information before approving an alternative lancet.
The current product page presents selected purple-device configurations with vacuum-assisted support, adjustable penetration depth, top-button activation and compatible-lancet use. Exact mechanism, settings and instructions should be confirmed by SKU.
Selected purple-device configurations are presented with a vacuum-assisted sampling feature. Confirm the exact contact-head design, intended function and operating instructions against the quoted device and current IFU.
Selected configurations include an adjustable depth mechanism. Confirm the number of settings, dial markings and operating range for the exact ELD-1 configuration being supplied.
The current product presentation includes a top-mounted activation button. Loading, cocking, activation and reset steps should follow the instructions supplied with the exact device.
The published ordering table currently lists BL-30G / BL-30E as the compatible-lancet entry. Final compatibility should be confirmed against the device configuration and current product documentation before purchase.
A purple lancing device should be purchased as a defined device configuration, not by color alone. Confirm the ELD-1 reference, depth-adjustment configuration, compatible lancet, labeled use condition, packaging and documentation before approving the SKU.
Confirm ELD-1, ELD-2.0 and the exact supplied configuration.
Confirm adjustment settings, activation and operating sequence.
Confirm BL-30G / BL-30E or the approved alternative by SKU.
Confirm 1/box, 20/case, labeling, IFU and required records.
For reusable blood-lancet or fingerstick devices, verify the current product labeling and IFU for the intended market. U.S. FDA guidance recommends that devices designed for repeated use be limited to multiple uses in only a single patient.
Product-level documentation review, selected U.S.-warehouse-supported fulfillment, packaging coordination and recurring device-plus-lancet supply planning for qualified B2B requirements.
Review specifications, compatible-lancet information, packaging, labeling, IFU and available quality or regulatory records against the exact device and project.
Documentation Support →Selected inventory can be reviewed for domestic fulfillment according to exact SKU, pack quantity, lot information, destination and current availability.
Fulfillment Support →Eligible packaging, artwork and labeling projects can be reviewed against the selected device, order volume, target market and documentation requirements.
Packaging Program →Coordinate the reusable device and compatible disposable lancet as one replenishment program with separate SKU and case controls.
View Blood Lancets →Compare the purple and white device families by model identity, depth adjustment, compatible lancet, operating features and packaging before choosing the appropriate supply route.
Common procurement questions related to ELD-1, depth adjustment, compatible lancets, reusable-device use, packaging and bulk supply.
The current Tonmit product page lists the Purple Lancing Device as REF ELD-1 with Inside Code ELD-2.0. Final product identity, configuration and labeling should be confirmed on the quotation.
The current ordering table lists BL-30G with Inside Code BL-30E as the compatible-lancet entry. Confirm actual compatibility with the quoted ELD-1 configuration before ordering or substitution.
The current product information states that selected purple-device configurations may include adjustable penetration depth settings. Confirm the number of settings and exact mechanism by SKU.
The current ELD-1 ordering table lists 1 purple lancing device per box and 20 devices per case. Packaging revisions and final case configuration should be confirmed with the quotation.
For U.S. use, FDA guidance recommends that reusable blood lancet devices intended for repeated use be labeled for multiple uses in only a single patient. Always verify and follow the exact ELD-1 product label and IFU for the intended market.
Provide the ELD-1 device requirement, required quantity, target compatible lancet, packaging or labeling needs, destination, requested documentation and expected delivery schedule.
Share the required device quantity, compatible lancet requirement, destination, packaging, labeling and documentation needs for a model-specific supply review.