Logo
Luer adapter, 20G Pack of 100

Luer adapter, 20G Pack of 100

GBO (Greiner Bio-One)

Injection & Infusion
  • CE Marked medical device indicating conformity with applicable European medical device legislation.
  • Sterile, single Use device as stated in the official instructions for use.
  • Not made with natural rubber latex or DEHP, supporting compatibility with latex Sensitive environments.
  • Manufactured and distributed within the Greiner Bio One VACUETTE preanalytics quality system (Greiner Bio One operates under ISO Certified quality management for medical devices).
Venous blood collection accessories / Luer adapters

Description

The VACUETTE Luer Adapter 20G is a sterile, single-use, non-invasive medical device used as a connector in venous blood collection. Supplied as a pack of 100, each 20G luer adapter is designed for use with VACUETTE tube holders and compatible winged or luer needles to allow safe and reliable venous blood collection into one or multiple blood collection tubes for in vitro diagnostic testing in hospitals, clinics and laboratories. The adapter is manufactured from stainless steel and polypropylene, is not made with natural rubber latex or DEHP, and incorporates a safety valve and perforated integrity seal to help prevent leakage and maintain sterility.

Bnefits

  • Provides a secure luer connection between VACUETTE tube holders and compatible winged or luer needles for venous blood collection.
  • Sterile, single-use device reduces risk of cross-contamination and healthcare-associated infections.
  • Manufactured from stainless steel and polypropylene, and not made with natural rubber latex or DEHP, supporting use in latex-sensitive patients and staff.
  • Integrated safety valve and perforated seal support product integrity and help minimise blood exposure and leakage.
  • Standard 20G size compatible with common venous blood collection practices.
  • Designed as part of the VACUETTE preanalytics system for reliable sample collection for in vitro diagnostic testing.
  • Supplied in packs of 100 for efficient stocking in hospitals, clinics and laboratories.

Indications

  • Venous blood collection in combination with VACUETTE tube holders and compatible winged needles or luer needles.
  • Collection of blood samples into one or multiple VACUETTE blood collection tubes for in vitro diagnostic testing.
  • Use in healthcare settings such as hospitals, clinics, laboratories and other medical facilities where venous blood sampling is performed.
  • Use in the general patient population where venous blood collection is required.

Composition

  • Adapter manufactured from stainless steel and polypropylene.
  • Fitted with a safety valve at one end to help prevent blood leakage.
  • Perforated label acting as both an identification aid and integrity seal.
  • Not made with natural rubber latex.
  • Not made with DEHP (di-2-ethylhexyl phthalate).

Formulation

  • Sterile, single-use, non-invasive medical device intended for venous blood collection.
  • VACUETTE 20G luer adapter designed to be used with VACUETTE tube holders and compatible butterfly or luer needles.
  • Non-ridged design with 20G lumen to support standard venous collection techniques.
  • Sterilised using ethylene oxide (EO) as indicated in the instructions for use.
  • CE-marked medical device for use within the VACUETTE preanalytics system.

Packaging

  • Pack of 100 VACUETTE Luer Adapter 20G units (Medisave product configuration).
  • Individual adapters supplied sterile in primary packaging with perforated integrity label.
  • Outer carton labelled with product name, brand (GBO / VACUETTE), item number 450070 and quantity.
  • Larger manufacturer packing configurations available (up to 6000 units per shipping carton), but the Medisave retail pack is 100 adapters.

Usage

  • For use by properly trained healthcare professionals only and in accordance with the VACUETTE instructions for use and local facility protocols.
  • Before use, inspect the packaging and perforated label: do not use if the label is broken, packaging is damaged or unintentionally opened, or if the product is past its expiry date.
  • Grasp both ends of the luer cover and carefully twist to break the perforated label seal.
  • Remove the shorter end of the cover and thread the luer adapter securely into a compatible VACUETTE tube holder, ensuring it is firmly seated.
  • Remove the longer end of the cover from the luer adapter and attach a compatible winged needle or luer needle as per facility procedure.
  • Select and prepare the venipuncture site using appropriate antiseptic; apply a tourniquet for no longer than recommended (typically up to 1 minute).
  • Perform venipuncture and collect blood according to facility procedures, inserting blood collection tubes into the holder and maintaining sufficient pressure to ensure full vacuum draw.
  • Follow facility guidance regarding use of discard tubes for tests sensitive to underfilling.
  • After blood collection is complete, remove the device and promptly dispose of the luer adapter (and associated needle set) in an approved sharps/biohazard container.
  • Do not reuse or resterilise the luer adapter under any circumstances.

Contraindications

  • Do not use in patients or staff with known hypersensitivity to any component of the device (e.g., stainless steel, polypropylene) where such exposure is clinically relevant.
  • Not validated for use with arterial or venous catheters; should not be used for these applications.
  • Do not use if packaging is damaged, if the perforated label is broken before intended use, or if storage conditions have been exceeded.
  • Do not use after the indicated expiration date.
  • Device is specifically designed for use within the VACUETTE system; safety and performance are not confirmed when used with non-Greiner components.

Adverse Effects

  • As a blood collection accessory, potential indirect risks include needlestick injury and exposure to bloodborne pathogens (e.g., HIV, hepatitis viruses) if not handled and disposed of correctly.
  • Improper use may result in blood leakage or incomplete tube filling, which can lead to erroneous laboratory results and possible inappropriate clinical decisions.
  • Very rare risk of local reactions associated with venipuncture (e.g., bruising, haematoma, pain) related to the blood collection procedure rather than the adapter itself.
  • Reuse or resterilisation, contrary to instructions, may lead to cross-contamination and transmission of infectious diseases.

Storage Conditions

  • Store at 4–36 °C (40–97 °F).
  • Avoid exposure to direct sunlight.
  • Keep dry and within the recommended temperature range to avoid impairment of product performance.
  • Do not use if storage conditions have been exceeded or if packaging shows signs of damage.
  • Keep in original packaging until point of use and store out of reach of unauthorised personnel.

Duration

Onset

Browse more Injection & Infusion

Top Treatments

Top Cities in the UK