Edge Safety Needle Pink   18G x 38 mm (1 1/2\) x 1000

Edge Safety Needle Pink 18G x 38 mm (1 1/2\) x 1000

Needle-Pro EDGE

Injection & Infusion
  • CE Marked sterile, single Use safety hypodermic needle device (medical device, not a medicinal product).
  • Safety Engineered device designed to meet NIOSH/CDC recommendations for needlestick injury prevention.
  • Colour coding conforms to ISO standard colour identification for needle gauge sizes.
  • Manufactured under a certified medical device quality management system (e.g. ISO 13485) by ICU Medical / Smiths Medical.
  • Complies with applicable sharps safety regulations and occupational health guidelines in relevant markets.
Safety hypodermic needles

Description

The Edge Safety Needle Pink - 18G x 38 mm (1 1/2\) x 1000 is the Jelco Hypodermic Needle-Pro EDGE safety hypodermic needle from ICU Medical (formerly Smiths Medical). It is a sterile, single-use hypodermic needle with a hinged, manually activated safety sheath designed to help protect clinicians from needlestick injuries. The 18G, 38 mm (1.5 inch) stainless steel needle is colour-coded pink in accordance with ISO gauge standards. The integrated Needle-Pro EDGE safety mechanism is activated with a simple one-handed technique after injection: the needle is locked inside the protective sheath with an audible click and the entire device is then disposed of in a sharps container. The device is engineered to provide cost-effective, safety-engineered solutions for routine hypodermic injections and fluid withdrawal in a wide range of clinical applications while minimising dead space and maintaining clear bevel orientation and bold, distinct syringe markings.

Bnefits

  • Integrated safety-engineered design to help reduce potential for needlestick injuries by minimising critical exposure time.
  • Simple, one-handed activation of the hinged safety sheath for ease of use and compliance with sharps safety protocols.
  • Low dead space design to minimise medication waste during injection or aspiration.
  • Bold, distinct syringe markings (when used with matching EDGE safety syringe) to support accurate dosing.
  • Bevel orientation indicator and fixed bevel-up position to support consistent needle positioning.
  • Entire device colour-coded to ISO standard gauge colours for rapid identification (pink for 18G).
  • Sterile, single-use device designed to meet NIOSH/CDC recommendations for needle safety devices.
  • Engineered for cost-effective sharps safety while maintaining clinical performance.

Indications

  • For hypodermic injection of fluids such as medications, vaccines and other parenteral solutions.
  • For withdrawal of blood or other body fluids via hypodermic access when clinically indicated.
  • Use in general medical, surgical, emergency, anaesthetic and outpatient settings where an 18G needle is appropriate.
  • Applications requiring a larger-bore needle for rapid injection or aspiration, reconstitution and drawing up of viscous medications or solutions.
  • Use where a manual, hinged safety needle is required to support sharps injury prevention policies.

Composition

  • Stainless steel hypodermic needle cannula (18G, 38 mm) with regular bevel.
  • Plastic hub with standard Luer connection compatible with standard Luer syringes.
  • Integrated hinged plastic safety sheath (Needle-Pro EDGE mechanism) attached to the needle hub.
  • Latex-free construction (no natural rubber latex in fluid-contact or handling components).

Formulation

  • Sterile, single-use safety hypodermic needle device with hinged mechanical safety shield.
  • Supplied non-pyrogenic and latex-free, individually packaged in peel-open blister packs.

Packaging

  • Individually sterile blister-packed safety needles.
  • 100 needles per box.
  • 10 boxes per shipping case (total 1000 needles per case for code 401815).
  • Outer case labelled with product code 401815, gauge/length (18G x 1.5"), colour (pink), lot number and expiry date.

Usage

  • Open the sterile blister pack immediately before use and remove the device without touching the needle or safety sheath.
  • Attach the Luer hub of the safety needle securely to a compatible Luer syringe, taking care not to damage the safety mechanism.
  • With the needle bevel up, remove the needle cap by pulling it straight off without twisting, and draw up medication as required.
  • Expel any air from the syringe and administer the injection according to local clinical protocols and best practice.
  • After withdrawal of the needle from the patient, keep your free hand behind the needle at all times and do not attempt to recap.
  • Activate the Needle-Pro EDGE safety mechanism using a one-handed technique by gently pressing the safety sheath against a flat, stable surface until an audible click confirms the needle is locked inside the sheath.
  • Visually confirm that the needle tip is fully engaged within the protective sheath and cannot be exposed.
  • Immediately dispose of the entire device (needle and syringe) in an approved sharps container after activation.
  • Do not reuse, re-sterilise, bend or break the needle before disposal.

Contraindications

  • Do not use if the sterile package is open, damaged or has been previously compromised.
  • Not for reuse; single-use only. Reuse may lead to infection, dullness or failure of the safety mechanism.
  • Do not use in patients with known hypersensitivity or allergy to stainless steel or any material in the device.
  • Not suitable for use in applications requiring specialised needles (e.g. spinal, epidural, intravenous catheter placement) where product-specific devices are recommended.
  • Do not use if the safety mechanism appears damaged or does not function as described in the instructions for use.

Adverse Effects

  • Local pain, bruising or minor bleeding at the injection site, as with all hypodermic needle procedures.
  • Potential for local tissue trauma or haematoma if insertion technique is suboptimal.
  • Risk of local infection or abscess formation at the injection site if aseptic technique is not followed.
  • Rare hypersensitivity or allergic reactions to device materials in susceptible individuals.
  • Potential needlestick injury to healthcare workers or others if the safety mechanism is not correctly activated or the device is mishandled.

Storage Conditions

  • Store in a clean, dry environment at room temperature, away from excessive heat and direct sunlight.
  • Keep in original packaging until point of use to maintain sterility and protect the safety mechanism.
  • Do not expose the sterile packs to moisture or chemicals that could compromise packaging integrity.
  • Do not use beyond the expiry date indicated on the packaging.
  • Keep out of the reach of children and unauthorised personnel.

Duration

Onset

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