M-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, irradiation sterilization, one-step activation, post-activation needle retraction, packaging and available documentation before approving a SKU.
21G, 23G, 28G and 30G
Length is controlled by REF
Current published method for listed SKUs
Qty/Box · Qty/Case
Gauge and needle length are not interchangeable purchasing fields. Use the exact REF and inside code in quotations, artwork and purchase orders, and verify sterilization, packaging, labeling and intended-use documentation against the selected configuration.
The table below follows the current Tonmit M-Type ordering data. Final labeling, lot information and available documentation should be confirmed with the quotation.
| REF / SKU | Inside Code | Needle Gauge | Needle Length | Sterilization | Qty / Box | Qty / Case |
|---|---|---|---|---|---|---|
| SL-21-24M | SL-21-24M2 | 21G | 2.4 mm | Irradiation | 100 | 2,000 |
| SL-23-18M | SL-23-18M2 | 23G | 1.8 mm | Irradiation | 100 | 2,000 |
| SL-28-18M | SL-28-18M2 | 28G | 1.8 mm | Irradiation | 100 | 2,000 |
| SL-30-18M | SL-30-18M2 | 30G | 1.8 mm | Irradiation | 100 | 2,000 |
A controlled RFQ should identify the exact REF, gauge, needle length, activation method, post-use safety mechanism, sterilization, package identity and intended sampling workflow. Do not infer blood sample volume or penetration performance from gauge alone.
Current M-Type product information highlights a shielded needle, post-activation retraction, tri-bevel needle tip and one-step activation. Treat each feature as part of the exact SKU and confirm the applicable instructions and product documentation before procurement.
The current M-Type product design keeps the needle enclosed before use. Confirm protective-cap handling, activation preparation and the exact pre-use state in the current IFU for the selected REF.
Selected M-Type configurations use an internal retraction mechanism after activation to reduce exposure of the used sharp. Confirm the irreversible post-use state and disposal instructions by REF.
Selected M-Type safety lancets are presented with a tri-bevel needle tip. Gauge and needle length remain the primary published ordering fields; any additional performance or comfort claim should be supported by the exact product specification.
The current M-Type page describes one-step activation without a separate pre-loading step. Confirm cap removal, positioning, activation sequence and post-use handling in the IFU for the exact quoted configuration.
“M-Type safety lancet” is a product family, not a complete purchase specification. Confirm the REF, gauge, needle length, activation and retraction mechanism, sterilization, packaging, intended use and required documentation before approving a substitution.
Confirm the exact REF, inside code, gauge and published needle length.
Confirm one-step activation, pre-use shielding and post-use retraction by SKU.
Verify irradiation method, sterile barrier, label revision, IFU and shelf-life data.
Confirm 100/box, 2,000/case, order quantity, destination and fulfillment requirements.
For assisted blood glucose monitoring, CDC recommends single-use, auto-disabling fingerstick devices and specifically recommends selecting single-use lancets that permanently retract after puncture. Confirm that the exact M-Type SKU, labeling and intended use support the planned healthcare 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 lancet supply planning for qualified B2B procurement programs.
Review specifications, irradiation information, labeling, IFU, packaging and applicable product documentation against the exact M-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, activation method, standard versus safety-lancet workflows, assisted monitoring requirements and RFQ fields before standardizing a lancet SKU.
Common procurement questions related to M-Type REF codes, gauge, needle length, irradiation, activation, retraction and packaging.
The current M-Type page lists four 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 published configurations include 1.8 mm and 2.4 mm needle lengths. SL-21-24M is listed as 21G × 2.4 mm, while the 23G, 28G and 30G listed M-Type configurations use 1.8 mm.
The current Tonmit M-Type page describes these products as single-use sampling devices with a shielded needle and post-activation retraction on selected configurations. Confirm the exact labeling and IFU for the quoted REF.
All four currently published M-Type REF rows list irradiation as the sterilization method. Buyers should confirm the exact sterile barrier, sterilization record, shelf-life information and label revision for the supplied lot and SKU.
The current ordering table lists 100 pieces per box and 2,000 pieces per case for the four published M-Type configurations. Final carton, artwork and shipping details should be confirmed in the quotation.
Provide the target REF or gauge × needle length, estimated quantity, intended sampling setting, sterilization and packaging requirements, 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.