Logo
EVAC S Single Use Suction Device

EVAC S Single Use Suction Device

Timesco EVAC-S

Medical device
  • CE marked medical device for suction of the oro Pharynx in line with relevant European/UK medical device regulations.
  • Manufactured under an ISO 13485 Certified quality management system for medical devices.
  • Produced by Timesco Healthcare Ltd, a long Established medical device manufacturer and supplier to the NHS and other healthcare systems.
  • Supplied sterile and single Use to support infection prevention and control policies in healthcare environments.
Single-use manual suction device for airway/oro-pharyngeal suction

Description

The EVAC-S Single-Use Suction Device is a sterile, completely single-use, manual hand-held suction device designed for effective oro-pharyngeal suction in emergency and clinical settings. Supplied with a 300 ml collection canister, adult and paediatric catheters, and a self-seal disposal polybag with a peel-off biohazard label, it provides a portable, one-handed solution for clearing the airway while minimising cross-contamination risk. The device delivers a maximum vacuum of 500 mmHg with a peak free airflow greater than 20 ml, and is CE marked and manufactured under an ISO 13485 quality management system. It is typically supplied as Timesco model TDM-ESD-100, often in boxes of five devices.

Bnefits

  • Completely single-use design eliminates the need for reprocessing and minimises cross-contamination risk.
  • Manual, hand-held, lightweight and portable device suitable for emergency, pre-hospital and clinical environments.
  • High vacuum performance up to 500 mmHg with peak free airflow greater than 20 ml, supporting effective oro-pharyngeal suction.
  • Includes both adult and paediatric catheters, allowing use across a wide range of patient ages within appropriate clinical protocols.
  • Supplied with a 300 ml sealed disposable canister and overflow protection to reduce the risk of leakage or spillage when full.
  • Self-seal disposal polybag with peel-off biohazard label simplifies safe post-use containment and waste segregation.
  • Wide operating temperature range (approximately -20 °C to +50 °C) and storage range (-40 °C to +60 °C) support use and storage in diverse environments, including pre-hospital and field settings.
  • CE marked and manufactured under ISO 13485, supporting compliance with relevant medical device quality and regulatory standards.

Indications

  • Emergency oro-pharyngeal suction to clear blood, vomit, secretions and other fluids from the upper airway.
  • Airway management in resuscitation, trauma, cardiac arrest and other acute medical emergencies.
  • Use on resuscitation trolleys, emergency grab bags, ambulances, military, maritime, mountain rescue and other pre-hospital settings by trained personnel.
  • Short-term suction support in clinical areas such as accident and emergency departments, minor treatment rooms and urgent care, where a simple, disposable suction solution is required.
  • Use as a backup or alternative suction method where powered suction units are unavailable, impractical or have failed.

Composition

  • Hand-held manual suction pump with integrated handle and suction mechanism (material details not publicly specified).
  • 300 ml disposable collection canister with integrated cap and suction port (external diameter approximately 17 mm).
  • Adult suction catheter (approximate external diameter 9 mm).
  • Paediatric suction catheter (10 French gauge, 10 fg).
  • Self-seal disposal polybag with two-ply label including peel-off biohazard warning for disposal.
  • One-way valves and overflow protection integrated into the cap/canister assembly (detailed internal materials and valve design not publicly specified).

Formulation

  • Single-use, sterile, manual mechanical suction device for oro-pharyngeal suction.
  • Hand-operated pump mechanism designed for one-handed operation, leaving the other hand free for patient management.
  • Mechanical design incorporates one-way valves and overflow protection to reduce backflow and spillage when the canister is full.
  • Non-powered, self-contained device requiring no external power source, battery or compressed gas.

Packaging

  • Individual sterile device supplied in a polybag with two-ply label that converts to a biohazard label after use.
  • Box contents per unit: 300 ml canister, adult catheter, paediatric catheter, self-seal disposal polybag, biohazard label, multilingual product instructions and multilingual labelling.
  • Timesco master packaging configuration described as supplied in boxes of 5 EVAC-S devices.
  • Outer cartons suitable for bulk storage and distribution via medical supply chains.

Usage

  • Use only by trained healthcare professionals or first-aiders trained in suction and airway management, following local clinical protocols.
  • Remove the device from its packaging and identify the appropriate catheter (adult or paediatric) based on patient size and clinical need.
  • Connect the catheter securely to the suction port on the cap/canister assembly (approximately 17 mm external diameter port).
  • Position the catheter correctly in the oro-pharynx as per local airway management guidelines and operate the manual pump handle to generate suction (up to 500 mmHg).
  • Monitor canister fill level; the built-in overflow protection will engage once the canister approaches full capacity to minimise leakage or spillage.
  • On completion of suction, withdraw the catheter carefully, maintaining infection control precautions, and disconnect from the patient.
  • Place the entire used device (including canister and catheter) back into the self-seal polybag, seal the bag, and peel the outer layer of the label to reveal the biohazard warning.
  • Dispose of the sealed biohazard-labelled bag in accordance with local clinical waste policies for infectious or potentially infectious material.
  • Do not attempt to clean, disinfect, or re-use the device; it is designed strictly for single use only.
  • Store unused devices in their original packaging within the specified temperature ranges and away from direct sunlight, moisture and mechanical damage.

Contraindications

  • Do not use in patients or situations where oro-pharyngeal suction is clinically contraindicated according to local guidelines (e.g. certain facial or airway traumas where suction could worsen injury).
  • Not intended for tracheal or deep bronchial suction beyond the manufacturer’s and institutional clinical protocols.
  • Do not use if sterile packaging is damaged, opened prior to use, or if any part of the device appears damaged, deformed or contaminated before first use.
  • Do not re-use on another patient or re-use on the same patient after initial use; the device is strictly single-use.
  • Do not connect to any external vacuum source or modify the device, as this may compromise performance and safety.
  • Not intended for use outside the specified operating temperature range (-20 °C to +50 °C) or in environments that cannot support appropriate infection control and clinical waste disposal.

Adverse Effects

  • Potential for oral or pharyngeal mucosal trauma, bleeding or discomfort if the catheter is inserted or manipulated incorrectly or with excessive force.
  • Possible gagging, coughing or vomiting associated with oro-pharyngeal suction in awake or semi-conscious patients.
  • Risk of cross-infection if the device is misused (e.g. re-used between patients) or if local infection control procedures are not followed.
  • Spillage or leakage of aspirated material if the device is overfilled, used with damaged components, or disposed of incorrectly, potentially creating environmental contamination hazards.
  • General risks associated with airway interventions, including potential transient hypoxia or bradycardia, if suctioning is prolonged or performed without adequate monitoring, emphasising the need for trained operators and adherence to clinical guidelines.

Storage Conditions

  • Store unused devices within the recommended storage environmental temperature range of approximately -40 °C to +60 °C.
  • Use the device within the specified operating environmental temperature range of approximately -20 °C to +50 °C for optimal performance.
  • Keep in original packaging until point of use to maintain sterility and protect against dust, moisture and physical damage.
  • Store in a clean, dry area away from direct sunlight, chemicals or sharp objects that could compromise packaging integrity.
  • Rotate stock according to expiry dates and local inventory policies to ensure devices are used within their shelf-life.

Duration

Intended for short-term episodic use during an emergency or clinical suction procedure only; not designed for continuous or long-term suction therapy.

Onset

Immediate mechanical effect during operation of the hand pump, with suction available as soon as the catheter is connected and the device is activated.

Browse more Medical device

Top Treatments

Top Cities in the UK