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QLICKSMART UNIT

Product information

  • Quantity Unit Single
  • Product Code None

$40.04 incl GST

Description

The Qlicksmart BladeNeedleSYSTEM is an innovative dual-function safety device tailored for surgical environments. Designed by Qlicksmart, it seamlessly integrates the safe removal of scalpel blades with the essential task of counting and disposing of suture needles. This device enhances safety and efficiency in operating rooms through its intuitive single-handed operation.

Key Features

  • Scalpel Blade Removal: The device employs a simple push, click, and pull mechanism, allowing for the swift and secure removal of scalpel blades. Each unit is equipped with two cartridges, with each cartridge capable of removing one blade. Post-use, these cartridges are intended for single use only and should be disposed of as medical waste.

  • Needle Counter: The needle counter features a numbered foam block and a magnetic surface, accommodating odd-shaped sharps. This ensures accurate needle counting and secure disposal, reducing the risk of sharps injuries.

Compatibility

The BladeNeedleSYSTEM is compatible with a wide range of scalpel handles, including models #3, 3L, 4, 4L, 5, 7, 9, baron, and cylindrical. It supports various scalpel blades such as #10, 10a, 11, 11P, 12, 14, 15, and many others. However, it is not compatible with Beaver handles or disposable handles.

Material and Sterilization

Constructed from high impact polystyrene for the needle counter box and polypropylene for the cartridges, the device is robust and reliable. It is sterilized using gamma radiation and is both latex and DEHP free, ensuring it meets the stringent hygiene standards required in medical settings.

Dimensions and Weight

  • Closed Dimensions: 11.7 cm x 6.6 cm x 3.9 cm
  • Open Dimensions: 11.7 cm x 12.7 cm x 8.7 cm
  • Weight: 51 g

These compact dimensions and lightweight design make it a convenient addition to any surgical toolkit.

Regulatory Compliance

The Qlicksmart BladeNeedleSYSTEM is compliant with international medical device standards, holding TGA ARTG listing in Australia, FDA listing in the USA, and CE marking in Europe. It also adheres to the AS 3825:2020 standard, underscoring its commitment to quality and safety in surgical practice.

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