PRESSURE-ACTIVATED SAFETY LANCETS

T-Type Safety Lancets with Automatic Needle Retraction

Sterile single-use safety lancets for capillary blood sampling. T-Type models are pre-loaded and pressure activated, with the needle shielded before use and retracted back into the device body after activation.

01 Pressure Activated

Pre-loaded contact activation without a separate lancing device.

02 Automatic Retraction

Spring-loaded mechanism returns the needle into the device after activation.

03 Gamma Sterilized

Current manufacturer T-Type information specifies gamma irradiation sterilization.

T-Type single-use safety lancets in multiple color-coded configurations
PUBLISHED REFS 5 T-Type SKUs

21G, 23G, 28G and 30G

NEEDLE LENGTH 1.8 / 2.4 mm

Published as needle length by REF

ACTIVATION Pressure Activated

Pre-loaded standalone safety lancet

PACKAGING 100 / Box · 1,000 / Case

Published T-Type case configuration

EXACT-SKU ORDERING DATA

T-Type Safety Lancet Specifications by REF

Order the T-Type family by exact REF, gauge and published needle length. The 1.8 mm and 2.4 mm values below are manufacturer-listed needle lengths, not automatically equivalent to controlled skin penetration depth.

REF / SKU 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
BUYER CONTROL Use the full REF in quotations, artwork and purchase orders so gauge, needle length and pack configuration remain tied to the same SKU.

T-TYPE PRODUCT DIFFERENCES

What Defines the T-Type Safety Lancet

The T-Type format combines pressure activation, post-activation needle retraction, a shielded needle architecture and gamma-irradiation sterilization.

T-Type safety lancet showing the pressure-activated contact end
01 / ACTIVATION

Pre-Loaded Pressure Activation

The T-Type device is supplied pre-loaded. After the protective cap is twisted and removed, the contact end is positioned against the sampling site and pressed to activate.

T-Type safety lancet with needle enclosed inside the device body
02 / POST-USE SAFETY

Automatic Needle Retraction

U.S. model records describe a spring-loaded mechanism that drives the needle forward and then withdraws it back into the device shield after activation.

T-Type safety lancet representing gamma irradiation sterilization
03 / STERILIZATION

Gamma Irradiation Sterilization

Current manufacturer T-Type product information identifies gamma irradiation as the sterilization method for the published family.

Close-up view of a tri-bevel needle tip used in T-Type safety lancets
04 / NEEDLE GEOMETRY

Tri-Bevel Needle Tip

The manufacturer describes a tri-bevel needle-tip geometry across the T-Type family while gauge and needle length remain the key ordering controls.

PRESSURE-ACTIVATION WORKFLOW

From Cap Removal to Sample Collection & Disposal

T-Type is a pre-loaded standalone safety lancet. The protective cap is twisted and removed before use; pressure at the sampling site activates the mechanism, and the needle automatically returns into the shield after puncture.

01
Twist & Remove the Protective Cap

Twist the protective cap as shown in the current IFU, then pull it away from the pre-loaded device.

02
Position the Contact End

Place the contact end firmly against the intended capillary sampling site.

03
Pressure Activate

Press the device against the sampling site to trigger puncture. The needle automatically returns into the shield after activation.

04
Remove the Device & Collect the Blood Sample

Lift the device away and collect the capillary blood sample according to the applicable sampling procedure.

05
Dispose After Single Use

Discard the used safety lancet in an appropriate sharps-disposal container according to local procedures.

MODEL-LEVEL IDENTITY

Selected Model-Level UDI Records

Selected T-Type models have current U.S. GUDID records under the Verifine brand. The records shown below are not a complete T-Type family list; match each Primary DI to the exact model string and current product label used for the quoted configuration.

SL-28-18T 00850011833452
SL-23-18T 00850011833377
SL-21-18T 00850011833285
SL-21-24T 00850011833315

Primary DI values shown above are selected model-level U.S. records and should be matched against the exact current label before use in procurement systems.

PROCUREMENT FILE CATEGORIES

Documents Available for Review

Product Specification

Exact REF, gauge, manufacturer-listed needle length, activation format and packaging configuration.

Instructions for Use

Cap removal, pressure activation, post-use needle state and disposal instructions.

Sterilization Information

Applicable gamma-irradiation and sterile-barrier records for the quoted product configuration.

Packaging & Label Files

Unit packaging, case quantity, label sample, barcode and private-label artwork where applicable.

Regulatory & UDI Records

Applicable manufacturer regulatory references and model-level UDI records for the target market.

T-TYPE SAFETY LANCET RFQ

Request T-Type Safety Lancet Bulk Pricing

Send the required REF, gauge × needle length, quantity, destination, packaging or private-label requirements and document needs for a SKU-specific quotation.

Submit T-Type Requirements