Heel blood lancets for professional pediatric and clinical blood sampling supply programs. Review the exact REF, listed use category, puncture depth, blade width, EO sterilization, protective-key configuration, box quantity and case pack before approving a product.
Four listed product configurations
Depth is controlled by exact REF
Width varies with selected configuration
Current listed standard pack
Current heel blood lancet specifications are organized by REF rather than gauge. Control the listed use category, color, puncture depth, blade width, sterilization and pack hierarchy against the exact SKU used in the quotation and purchase order.
Listed use categories below reproduce the current product-page information. Product selection remains subject to the applicable IFU, institutional protocol, clinician judgment and procurement requirements.
| REF / SKU | Listed Use Category | Color | Depth | Blade Width | Sterilization | Qty / Box | Qty / Case |
|---|---|---|---|---|---|---|---|
| HB-065 | <1000 grams | Purple | 0.65 mm | 1.50 mm | EO | 50 pcs | 500 pcs |
| HB-085 | Low birth weight | Green | 0.85 mm | 1.75 mm | EO | 50 pcs | 500 pcs |
| HB-100 | Birth up to 6 months | Blue | 1.00 mm | 2.50 mm | EO | 50 pcs | 500 pcs |
| HB-150 | 6-24 months | Gray | 1.50 mm | 3.00 mm | EO | 50 pcs | 500 pcs |
The purchase specification should identify the exact REF together with the listed use category, puncture depth, blade width, sterilization, packaging, current labeling and any required clinical or institutional approval.
Review structural and sterilization features together with the selected REF. Final performance, use category and labeling statements should remain tied to the exact product configuration and current instructions for use.
The current HB-065, HB-085, HB-100 and HB-150 specifications list EO sterilization. Review the current sterile barrier, lot, expiry and sterilization-related records when required for the selected SKU.
Selected heel lancet configurations use a protective-key and safety-catch structure around the activation area. Exact preparation and activation steps should follow the product IFU.
The housing includes textured grip surfaces and a compact hand-held form. Product dimensions, material and operating sequence should be confirmed against the selected REF when needed.
The corresponding product information describes an arc cutting blade intended to produce a small wound. Incision depth and blade width remain controlled by exact REF rather than by a generic family claim.
The public product record confirms a protective key and non-detachable safety catch, but it does not explicitly publish automatic blade retraction or an irreversible reuse lockout. Confirm the post-use blade state in the current IFU for the quoted REF.
The corresponding product instructions show manual preparation and trigger-button activation. Product selection, heel-site placement and post-collection care must follow the supplied IFU and applicable institutional protocol.
Prepare the device using its published protective control.
Place the device within the marked heel area according to the IFU.
Activate only after the device is correctly positioned and stabilized.
Use an appropriate sharps container and follow the stated site-care procedure.
Every returned file should identify the exact model or REF, responsible legal manufacturer or labeler, revision or effective date and applicable destination market.
Exact REF, incision dimensions, listed use category, activation sequence, post-use blade state, restrictions and disposal instructions.
Request REF Files →Current unit and box label, 50/box and 500/case hierarchy, lot, expiry, barcode fields and eligible private-label artwork.
Request Label Sample →Applicable EO sterilization evidence, sterile-barrier information, storage conditions and remaining shelf-life confirmation.
Request Sterility Index →Legal manufacturer or labeler, REF-to-UDI/DI mapping when applicable, destination-market record, document revision and validity.
Request Market Index →These families differ in penetrating element, purchasing specification, activation and external-device compatibility. They should not be treated as interchangeable catalog terms.
| Product Family | Primary Control | Activation | External Device | Published Distinction |
|---|---|---|---|---|
| Heel blood lancet | REF + depth × blade width | Safety-catch release + trigger button | Not required | Fixed blade for heel incision |
| T-Type safety lancet | REF + gauge × needle length | Pressure activated | Not required | Automatic needle retraction |
| M-Type safety lancet | REF + gauge × needle length | One-step activation | Not required | Shielded needle and post-use retraction |
| Twist-cap blood lancet | REF + gauge + loading format | Through compatible lancing device | Required | Separate lancet loaded into reusable device |
Provide the purchasing controls below so the quotation, label sample and document index resolve to the same product configuration.
Please enter the required REF, incision size and purchasing details yourself. This page does not insert text into the form.