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AIRWAY MANAGEMENT
VAPSAFE / VAPSAFE ULTRA — Endotracheal Tube with Subglottic Suction Line
VAPSAFE / VAPSAFE ULTRA — Endotracheal Tube with Subglottic Suction Line

VAPSAFE / VAPSAFE ULTRA — Endotracheal Tube with Subglottic Suction Line

Dedicated suction port removes subglottic secretions to minimise VAP

VAPSAFE / VAPSAFE ULTRA — Endotracheal Tube with Subglottic Suction Line is a sterile, single-use device manufactured from special non-toxic medical grade pvc, designed for maintaining a patent airway during prolonged ventilation or maxillofacial surgery, with reduced risk of ventilator-associated pneumonia or field-access obstruction.

ISO 5361
Latex Free
Sterile • Single-use
ISO 13485 • CE
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Overview

VAPSAFE / VAPSAFE ULTRA — Endotracheal Tube with Subglottic Suction Line is a sterile, single-use device manufactured from special non-toxic medical grade pvc, designed for maintaining a patent airway during prolonged ventilation or maxillofacial surgery, with reduced risk of ventilator-associated pneumonia or field-access obstruction. Direct VAP-reduction clinical claim.

Key features

Engineered for clinical confidence

Product Features

Subglottic Secretion Control

Dedicated suction port removes subglottic secretions to minimise VAP.

Product Features

Trachseal Cuff Aids Mucus-pool Formation

Trachseal cuff aids mucus-pool formation for effective suctioning.

Product Features

Ultra Adds Ultra-thin Polyurethane Microcuff

ULTRA adds ultra-thin polyurethane microcuff for improved seal at lower pressure.

Specifications

Technical data & ordering information

Intended use Maintaining a patent airway and mechanically ventilating patients during anaesthesia or critical care (nasal / oral).
Material / construction Special non-toxic medical grade PVC; PU microcuff on ULTRA variant
Sterilisation Sterile (ETO/EO sterilised), pyrogen-free; single patient use.
Packing Box of 25; Master Carton of 300
Master carton dimensions 660 x 380 x 500 mm (assumed — same tube family as SMD 722; confirm with QA)
Master carton gross weight 15.56 kg (assumed — same tube family as SMD 722; confirm with QA)

Variants & product codes

Available configurations under this product family

Product code Variant
SMD 722 VAPSAFE
SMD 722 UT VAPSAFE ULTRA

Clinical applications

Where this product is typically used

Operating theatre

Anaesthesia and airway/respiratory management during surgery.

Intensive care

Ventilated and critically ill patient management.

Emergency & ambulance

Acute airway/respiratory intervention.

Recovery & ward

Post-operative respiratory support.

Frequently Asked Questions

Common queries about VAPSAFE / VAPSAFE ULTRA — Endotracheal Tube with Subglottic Suction Line

VAPSAFE / VAPSAFE ULTRA — Endotracheal Tube with Subglot+BF21+BG21

Dedicated suction port removes subglottic secretions to minimise VAP, which supports safer, more comfortable use for both the clinician and the patient.

Yes — VAPSAFE / VAPSAFE ULTRA — Endotracheal Tube with Subglottic Suction Line is manufactured without natural rubber latex, making it suitable for use with latex-sensitive and latex-allergic patients.

Yes — VAPSAFE / VAPSAFE ULTRA — Endotracheal Tube with Subglottic Suction Line is manufactured from 100% DEHP-free medical-grade material, in line with current guidance on phthalate exposure in medical devices.

VAPSAFE / VAPSAFE ULTRA — Endotracheal Tub+BN21+BO21

VAPSAFE / VAPSAFE ULTRA — Endotracheal Tube with Subglottic Suction Line is manufactured to comply with ISO 5361, in addition to Sterimed's WHO-GMP, ISO 13485:2016 and CE-marked quality management system.

Downloads & Technical Resources

Access documentation and files for Steritrach Endotracheal Tube

Product Catalogue

Technical specifications, variants, and ordering details for VAPSAFE / VAPSAFE ULTRA — Endotracheal Tube with Subglottic Suction Line. (PDF — link to full E-Catalogue or SKU datasheet)

Download

Instructions for Use

Clinical guidelines, setup instructions, and safety information for VAPSAFE / VAPSAFE ULTRA — Endotracheal Tube with Subglottic Suction Line. (PDF — link to current IFU)

Download

Why clinicians choose Sterimed

Quality you can build a protocol around

Certified quality

Certified quality

Manufactured under WHO-GMP with ISO 13485:2016 and CE marking, EO-sterilised, pyrogen-free and lot-traceable.
Patient safety

Patient safety

DEHP-free and latex-free options, atraumatic design and single-use packaging support modern infection-control protocols.
Scale & supply

Scale & supply

In-house manufacturing since 1986 supports consistent supply for hospitals, tenders and large institutions.
Export & OEM ready

Export & OEM ready

Supplied to 50+ countries with private-label and OEM options, and documentation for regulatory submissions.

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