T-Type safety lancets for professional capillary blood sampling and diabetes-testing supply programs. Review the exact REF, 21G–30G gauge options, 1.8 mm or 2.4 mm needle length, gamma irradiation sterilization, pre-loaded pressure activation, shielded needle configuration, packaging and available documentation before approving a SKU.
21G, 23G, 28G and 30G
Length is controlled by REF
Pre-loaded T-Type design
Qty/Box · Qty/Case
Gauge and needle length must be controlled together with the exact REF. Use the full SKU in quotations, artwork and purchase orders, and verify sterilization, activation format, shielding, labeling and packaging against the selected configuration.
The table follows the current Tonmit T-Type ordering data. Final labeling, lot information, shelf life and available documentation should be confirmed with the quotation.
| REF / SKU | Needle Gauge | Needle Length | Sterilization | Activation | Qty / Box | Qty / Case |
|---|---|---|---|---|---|---|
| SL-30-18T | 30G | 1.8 mm | Gamma irradiation | Pressure activated | 100 | 1,000 |
| SL-28-18T | 28G | 1.8 mm | Gamma irradiation | Pressure activated | 100 | 1,000 |
| SL-23-18T | 23G | 1.8 mm | Gamma irradiation | Pressure activated | 100 | 1,000 |
| SL-21-18T | 21G | 1.8 mm | Gamma irradiation | Pressure activated | 100 | 1,000 |
| SL-21-24T | 21G | 2.4 mm | Gamma irradiation | Pressure activated | 100 | 1,000 |
A controlled RFQ should identify the exact REF, gauge, needle length, pressure-activation format, pre- and post-use needle state, sterilization, package identity and intended sampling workflow. Gauge alone does not establish penetration behavior, blood volume or suitability for a specific testing protocol.
Current T-Type product information highlights a fully shielded needle design, gamma irradiation sterilization, tri-bevel needle tip and pressure-activated operation. Confirm each feature against the exact REF, current labeling and applicable instructions for use.
The current T-Type page describes selected configurations with the needle shielded before and after use. Confirm the exact pre-use preparation, post-activation state and disposal instructions for the quoted REF.
All five currently published T-Type REF rows identify gamma irradiation as the sterilization method. Confirm the sterile barrier, lot release, shelf-life information and relevant sterilization records for the supplied SKU.
Selected T-Type configurations are presented with a tri-bevel needle tip. Gauge and needle length remain the published ordering controls; do not convert tip geometry into an unsupported comfort, blood-volume or performance claim.
T-Type safety lancets are currently described as pre-loaded, pressure-activated devices without a separate loading step. Confirm cap removal, positioning, activation pressure and post-use handling in the IFU for the exact SKU.
“T-Type safety lancet” identifies the family, not the final purchase specification. Confirm the REF, gauge, needle length, pressure activation, needle-shielding behavior, sterilization, packaging, intended use and required documentation before approving a substitute.
Confirm the exact T-Type REF, gauge and listed needle length.
Confirm the activation sequence and pre-/post-use needle state by SKU.
Verify gamma irradiation, sterile barrier, IFU, label revision and shelf-life data.
Confirm 100/box, 1,000/case, order quantity, destination and fulfillment requirements.
CDC recommends single-use, auto-disabling fingerstick devices in settings where assisted blood glucose monitoring is performed and recommends single-use lancets that permanently retract after puncture. Do not assume that pressure activation alone establishes these requirements. Confirm the exact T-Type SKU, labeling, post-use safety behavior and intended use for the planned setting, and dispose of used lancets at the point of use in an appropriate sharps container.
REF-level documentation review, selected U.S.-warehouse-supported fulfillment, packaging coordination and recurring safety-lancet supply planning for qualified B2B procurement programs.
Review specifications, gamma-irradiation information, labeling, IFU, packaging and applicable product records against the exact T-Type REF and destination market.
Documentation Support →Selected inventory can be reviewed by exact REF, pack quantity, destination and current availability before domestic replenishment or recurring supply is confirmed.
Fulfillment Support →Eligible unit packaging, cartons, artwork and labeling projects can be reviewed by REF, order volume, target market and documentation requirements.
Packaging Program →Coordinate safety-lancet supply with selected sharps-container formats for point-of-use disposal planning and recurring healthcare supply programs.
View Sharps Containers →Review gauge, needle length or fixed-depth concepts, standard versus safety-lancet workflows, activation method, assisted monitoring requirements, packaging and RFQ controls before standardizing a SKU.
Common procurement questions related to T-Type REF codes, gauge, needle length, gamma irradiation, pressure activation, shielding and packaging.
The current T-Type page lists five REF configurations covering 21G, 23G, 28G and 30G. Gauge should be ordered together with the exact REF and needle length rather than as a standalone field.
Current listed configurations include 1.8 mm and 2.4 mm. The 30G, 28G and 23G rows are listed at 1.8 mm; 21G is currently listed in both 1.8 mm and 2.4 mm REF configurations.
Yes. The current Tonmit page describes T-Type safety lancets as pre-loaded, pressure-activated devices. Confirm the activation sequence, required contact pressure and post-use device state from the IFU for the exact quoted REF.
All five currently published T-Type REF rows list gamma irradiation as the sterilization method. Confirm the applicable sterile barrier, lot-release information, shelf life and label revision for the supplied SKU.
The current ordering table lists 100 pieces per box and 1,000 pieces per case for all five published T-Type configurations. Final carton, artwork, barcode and shipping details should be confirmed in the quotation.
Provide the target REF or gauge × needle length, estimated quantity, intended sampling setting, activation and safety requirements, packaging, labeling or private-label needs, destination and requested product documentation.
Share the required REF, gauge × needle length, estimated quantity, packaging, labeling, destination and documentation requirements for a SKU-specific supply review.