Male Female Luer Lock Cap Pack of 100

Becton Dickinson

Medical consumable

IV / injection & infusion accessory \u2013 male/female Luer lock tip cap

Manufactured by Becton, Dickinson and Company in accordance with applicable medical device quality standards (e.g. ISO 13485).
Designed and marketed as a sterile single Use medical device accessory for Luer Compatible syringes and IV components.
Latex Free, DEHP Free and PVC Free material formulation, supporting allergy and safety Conscious clinical use.

Manufactured by Becton, Dickinson and Company in accordance with applicable medical device quality standards (e.g. ISO 13485).
Designed and marketed as a sterile single Use medical device accessory for Luer Compatible syringes and IV components.
Latex Free, DEHP Free and PVC Free material formulation, supporting allergy and safety Conscious clinical use.

IV / injection & infusion accessory \u2013 male/female Luer lock tip cap

Description

The BD Male-Female Luer Lock Cap (Pack of 100) is a sterile tip cap designed for safe closure of Luer-compatible syringes, connectors and open ports on intravascular devices such as infusion sets. Each cap incorporates both a male and a female Luer lock interface, allowing it to be used to close or couple compatible Luer ports as needed. Manufactured from medical-grade polypropylene and not made with natural rubber latex, DEHP or PVC, the cap helps minimise the risk of touch contamination and maintains a closed system during preparation, transport and short-term storage of IV lines and syringes. Tray-style packaging is used to reduce waste compared with individually pouched caps and to support quick, efficient aseptic application in clinical environments.

Bnefits

Provides sterile closure for syringes, connectors and open ports of intravascular devices such as infusion sets.
Male and female Luer lock design allows flexible use on a wide range of Luer-compatible ports and syringes.
Helps minimise touch-contamination risk during line preparation and handling.
Manufactured without natural rubber latex, DEHP or PVC – suitable for latex-sensitive environments.
Tray packaging supports efficient workflow and reduces waste compared to individually wrapped caps.
Designed for single use to support infection-prevention protocols in hospitals and clinics.

Indications

Temporary sterile closure of Luer lock syringe tips.
Closure of open Luer ports on IV sets, extension lines and other intravascular devices.
Protection of Luer connectors during preparation, transport and short-term storage.
Use in general hospital, theatre, critical care, outpatient and community settings where Luer-terminated devices are used.

Composition

Medical-grade polypropylene cap body.
Integral male Luer lock tip.
Integral female Luer lock connection.
Formulated without natural rubber latex.
Formulated without DEHP and PVC.
Colour variants commonly available in orange, blue or white depending on code/option.

Formulation

Non-medicated, non-sterile-contact (external) medical consumable component.
Supplied sterile and single use.
Compatible with standard Luer / Luer lock syringes and connectors (male and female).
Lipid-resistant material suitable for use with common IV fluids and many medications (per BD specifications).

Packaging

Pack of 100 BD Male-Female Luer Lock Caps.
Supplied in tray-style packaging to maintain sterility and facilitate aseptic removal.
Outer carton labelled with product description, brand (Becton Dickinson), SKU (TP-MF-O), quantity and lot/expiry information.
Non-sterile outer packaging; internal trays/compartments present caps in an orientation suitable for quick application.

Usage

Verify that the packaging and tray are intact and the product is within its expiry date before use.
Perform hand hygiene and use appropriate aseptic technique according to local infection-prevention policies.
Remove a tip cap from the tray taking care to avoid touching the surfaces that will be in contact with the Luer connector.
Attach the appropriate side (male or female Luer lock) firmly to the corresponding syringe tip or device port until secure.
Ensure the cap is fully seated and locked to maintain a closed, protective barrier.
Do not re-use caps; once removed, discard in an appropriate clinical waste or sharps container as per local policy.
Inspect lines and syringes before use to confirm that all caps are removed prior to connection to patients.

Contraindications

Do not use if packaging, tray or caps are damaged, visibly contaminated or beyond the indicated expiry date.
Not intended for use with non-Luer or non-compatible connectors.
Not suitable for reprocessing or reuse; re-use may increase risk of contamination or device failure.

Adverse Effects

If used incorrectly or if a cap is not removed prior to line use, there is a risk of obstruction of fluid flow.
Use of damaged or non-sterile caps may increase the risk of infection or contamination of IV systems.
Very rarely, hypersensitivity may occur to plastic materials, although the product is not made with natural rubber latex.

Storage Conditions

Store in a clean, dry environment at standard room temperature, away from direct sunlight and excessive heat.
Keep in original packaging until use to maintain sterility and protection from dust and contaminants.
Do not use if the product has been exposed to excessive moisture, heat or other conditions that could compromise integrity.
Store out of reach of children and non-clinical personnel.