B & D Microlance 3 Needles Blue 23G x 1.5 Inch Thin Wall (Box of 100)

Becton Dickinson

Injection and infusion devices

Sterile single-use hypodermic needles \u2013 23G thin wall

CE marked sterile hypodermic needle meeting applicable EU medical device requirements (CE marking via notified body as per BD Microlance 3 technical data sheet).
Manufactured under certified quality management systems including ISO 9001 and EN ISO 13485 for medical devices.
Conforms to EN ISO 7864 for sterile hypodermic needles for single use.
Conforms to EN ISO 9626 for stainless steel needle tubing for the manufacture of medical devices.
Colour coding according to EN ISO 6009 for hypodermic needles.
Sterilisation validated to EN ISO 11135 for EO Sterilised medical devices; sterility assurance level appropriate for single Use sterile products.
Complies with EN 556 1 requirements for medical devices labelled "sterile".
Latex Free and PVC Free; does not contain DEHP phthalates in the product as per BD declarations and REACH information.

CE marked sterile hypodermic needle meeting applicable EU medical device requirements (CE marking via notified body as per BD Microlance 3 technical data sheet).
Manufactured under certified quality management systems including ISO 9001 and EN ISO 13485 for medical devices.
Conforms to EN ISO 7864 for sterile hypodermic needles for single use.
Conforms to EN ISO 9626 for stainless steel needle tubing for the manufacture of medical devices.
Colour coding according to EN ISO 6009 for hypodermic needles.
Sterilisation validated to EN ISO 11135 for EO Sterilised medical devices; sterility assurance level appropriate for single Use sterile products.
Complies with EN 556 1 requirements for medical devices labelled "sterile".
Latex Free and PVC Free; does not contain DEHP phthalates in the product as per BD declarations and REACH information.

Sterile single-use hypodermic needles \u2013 23G thin wall

Description

B & D Microlance 3 Needles Blue 23G x 1.5 Inch - Thin Wall are sterile, single-use hypodermic needles from Becton Dickinson, designed for injection and aspiration of medical fluids. This configuration provides a 23 gauge (0.60 mm outer diameter) thin-wall stainless steel cannula with a length of 1½\ (40 mm), colour-coded blue and supplied in a box of 100. The Microlance 3 design features a triple-cut bevel, silicone lubrication and a precision-engineered cannula for smooth penetration and reduced tissue trauma, and is compatible with both Luer slip and Luer lock syringes.

Bnefits

Thin-wall 23G cannula (0.60 mm) allows improved flow rates compared with regular-wall needles of the same gauge.
Triple-bevel, ultrasonically polished stainless steel tip designed for smooth tissue penetration and reduced insertion force.
Silicone oil lubrication minimises friction for easier insertion and withdrawal and improved patient comfort.
Colour-coded polypropylene hub (blue for 23G) for quick and reliable gauge identification.
Compatible with both Luer slip and Luer lock syringes via standard 6% Luer taper.
Sterile, single-use and latex-free, reducing the risk of cross-contamination and latex-associated reactions.
EO (ethylene oxide) sterilised with validated process to EN ISO 11135 and a typical shelf life of 5 years.
Manufactured and tested to EN ISO 7864 and EN ISO 9626 standards for hypodermic needles and needle tubing.

Indications

Intended for the injection and/or aspiration of medical fluids, including body fluids (e.g. blood) and drugs, using compatible syringes.
Suitable for intramuscular, subcutaneous, intradermal or intravenous injections where a 23G x 40 mm needle is clinically appropriate.
Commonly used in general medical practice, hospitals, dental and aesthetic clinics and laboratory settings for injections and sample collection when compatible with procedure requirements.

Composition

Cannula: Stainless steel AISI 304 needle tubing, triple-cut bevel, thin wall, outer diameter 0.60 mm (23G).
Needle hub: Colour-coded polypropylene (blue for 23G).
Needle shield: Polypropylene protective cap.
Bonding agent: Epoxy resin to bond cannula to hub.
Lubricant: Medical grade silicone oil (<0.25 mg/cm²) on cannula for smoother insertion.
Packaging film: Polyamide web for individual sterile blister packs.
Outer box: Paperboard carton.
Materials of concern: PVC-free and DEHP-free; does not contain natural rubber latex (latex-free).

Formulation

Sterile, single-use hypodermic needle.
Gauge: 23G (0.60 mm outer diameter).
Length: 1½" (40 mm).
Wall type: Thin wall for enhanced flow.
Bevel: Regular triple-cut bevel for smooth penetration.
Colour code: Blue hub for 23G in accordance with EN ISO 6009.
Connection: Standard female Luer push-on (compatible with Luer slip and Luer lock syringes).
Sterilisation: Ethylene oxide (EO) sterilised.

Packaging

Supplied sterile in individual polyamide blister packs to maintain sterility until use.
Box of 100 needles per carton (standard BD Microlance 3 pack size).
Outer carton printed with gauge, length, colour code, lot number and expiry date.
Shelf life typically 5 years from date of manufacture when stored as recommended.

Usage

Single-use only; do not reuse. Reuse may lead to infection, needle blockage or reduced performance.
Select the appropriate gauge and length based on the clinical indication and patient requirements; 23G x 40 mm is commonly used for intramuscular and some subcutaneous or intravenous injections.
Inspect the sterile pack before use; do not use if the blister is opened, damaged or the expiry date has passed.
Attach the needle firmly to a compatible Luer slip or Luer lock syringe using the standard Luer taper connection.
Remove the protective needle shield immediately before injection, taking care to maintain sterility of the cannula.
Perform the injection or aspiration according to current clinical guidelines and local protocols for the intended route of administration.
After use, do not attempt to recap by hand; dispose of the used needle and syringe immediately into an approved sharps container in accordance with local regulations.
Store remaining needles in their original carton in a dry, clean area away from direct sunlight and sources of heat.

Contraindications

Do not use if the individual sterile package is damaged, open or contaminated, or if the product is past its expiry date.
Not suitable for use in patients with known hypersensitivity to any of the needle materials (e.g. stainless steel, silicone oil, epoxy), although true allergy is rare.
Use of a 23G x 40 mm needle may be inappropriate in very small, paediatric or emaciated patients where a shorter or finer gauge needle is indicated; select gauge/length according to clinical guidance.
Do not use for procedures or anatomical sites where this gauge and length could increase risk of nerve or vascular injury; follow local protocols for needle selection.
Do not reuse or resterilise; repeated use can cause loss of sharpness, increased pain, risk of breakage and infection transmission.

Adverse Effects

Local injection site reactions such as pain, bleeding, bruising, swelling or haematoma formation due to tissue trauma from needle insertion.
Very rare risk of needle-related complications such as nerve injury, vascular puncture or tissue damage if insertion technique or site selection is inappropriate.
Risk of infection or abscess formation at the injection site if aseptic technique is not followed.
Needlestick injury risk to healthcare workers if the needle is mishandled or disposed of incorrectly.
Hypersensitivity or allergic-type reactions to stainless steel, silicone oil or epoxy are possible but uncommon.
In extremely rare cases, needle bending or breakage can occur if excessive force is applied or the needle is manipulated improperly once inserted.

Storage Conditions

Store in a dry, warm place away from excessive humidity and moisture.
Protect from direct sunlight and strong light sources to maintain packaging integrity.
Keep in the original carton until use to protect the sterile blister packs.
Do not expose packaging to physical damage, crushing or puncture that could compromise sterility.
Observe the expiry date on the packaging; do not use after this date.
Keep out of the reach of children and unauthorised persons.

Duration

This is a sterile, single-use device used for a single injection or aspiration procedure and then safely discarded. It is not associated with a defined treatment duration; duration is determined by the medicinal product or procedure being administered.

Onset

Not applicable as the device itself has no pharmacological effect. The onset of clinical effect is determined by the medicinal product or fluid administered through the needle.