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Smiths Medical Portex Blue Line Ultra Plain Replacement Inner Cannula 100/850/060-100/850/090

Smiths Medical Portex Blue Line Ultra Plain Replacement Inner Cannula 100/850/060-100/850/090

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The Portex 100/850 is a plain (non-fenestrated) replacement inner cannula designed exclusively for use inside the Portex Blue Line Ultra outer tracheostomy tube. The inner cannula is the removable, cleanable tube that sits within the outer tracheostomy tube and forms the actual breathing channel for the patient. It carries all secretions, airway gases, and ventilator circuit connections — and must be kept clean and patent at all times to prevent life-threatening airway obstruction.

In active tracheostomy care, the inner cannula becomes coated with dried secretions and mucus over time. Removing it, cleaning it, and replacing it — or swapping in the second spare cannula while the soiled one is cleaned — is the single most important daily nursing task in tracheostomy management. The 100/850 replacement pack gives bedside nurses a ready supply of genuine, correctly-sized spare cannulae so that this rotation can continue without delay, even when a cannula becomes damaged or lost.

The plain design means there are no holes or openings in the cannula wall — making it the correct choice for any patient who is being mechanically ventilated, on CPAP, or who requires a sealed airway for any clinical reason. Patients on speaking valve trials or active weaning use the fenestrated variant (100/851) instead, under clinical direction.

Supplied across India by Shah Trading Corporation, Mumbai — trusted distributor and supplier of Smiths Medical Portex airway management products.

6.0 mm Tube - 100/850/060
7.0 mm Tube - 100/850/070
7.5 mm Tube - 100/850/075
8.0 mm Tube - 100/850/080
8.5 mm Tube - 100/850/085
9.0 mm Tube - 100/850/090

Key Features

* Exact-Match Replacement Design - Manufactured to the same dimensions and material specification as the inner cannulae supplied in the original Blue Line Ultra tracheostomy tube kit — ensuring a precise, secure fit in the outer cannula every time.

* Click-Lock Retention Mechanism - The inner cannula locks positively into the outer tube with an audible click. The tabs release with a simple squeeze-and-pull action — fast enough for emergency removal but secure enough to prevent accidental disconnection from ventilator circuits during patient movement or care.

* Smooth Inner Surface - The plain inner wall has a smooth bore that resists secretion adherence — slowing the rate of crust and mucus build-up inside the cannula. This extends the useful cleaning interval and reduces the risk of partial airway occlusion between cleaning cycles.

* Minimal Airway Diameter Reduction - The inner cannula reduces the effective airway lumen by just 1.0 mm across most sizes (1.5 mm for the 10.0 mm size only) — a clinically acceptable reduction that preserves adequate airflow and suction catheter passage without meaningfully increasing work of breathing.

Reference Outer Tube Size Inner Cannula ID Airway Reduction Pack Qty
100/850/060 6.0 mm 5.0 mm 1.0 mm 2 units
100/850/070 7.0 mm 6.0 mm 1.0 mm 2 units
100/850/075 7.5 mm 6.5 mm 1.0 mm 2 units
100/850/080 8.0 mm 7.0 mm 1.0 mm 2 units
100/850/085 8.5 mm 7.5 mm 1.0 mm 2 units
100/850/090 9.0 mm 8.0 mm 1.0 mm 2 units
100/850/100 10.0 mm 8.5 mm 1.5 mm 2 units

Specification

Parameter Detail
Type Plain (non-fenestrated) — sealed wall, no holes
Material Medical-grade soft, flexible PVC — same specification as Blue Line Ultra outer cannula
Surface Finish Smooth inner bore to resist secretion adhesion and simplify cleaning
Connector Standard ISO 15 mm at proximal end — universal ventilator circuit compatibility
Retention System Click-lock tab mechanism — audible engagement, squeeze-and-pull release
Colour Coding Clear / transparent — distinguishes plain from fenestrated (100/851 = red)
Compatible Outer Tubes Portex Blue Line Ultra® series: 100/810 (cuffed), 100/811 (uncuffed), 100/812 (cuffed fenestrated), 100/813 (uncuffed fenestrated), 100/815, 100/875 (Suctionaid)
Incompatible Tubes Do NOT use with Portex Corrugated Inner Cannula series (100/528, 100/522)
Maximum Period of Use 30 days per cannula (or discard if kinked, cracked, or visibly damaged before this)
Sterilisation Method Ethylene oxide (EO) — sterile as supplied
Latex Content Latex-free
DEHP Plasticiser Does not apply to this series — refer to product IFU for current data
Patient Population Adult (all sizes); paediatric sizes are a separate product line
Usage Classification Single-patient, reusable within the same patient during the recommended usage period
Cleaning Agent Sterile saline solution — do not use alcohol or abrasive agents on inner cannula
Storage Cool, dry place — keep packaging intact until point of use
Related Fenestrated Variant 100/851 (same size range — for weaning and phonation; red colour coded)
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Frequently Asked Questions

Why do we need replacement inner cannulae when two are already supplied with the tracheostomy tube kit?

The two inner cannulae included in every Blue Line Ultra kit are intended to support the rotation system — one in, one clean — during the initial period after insertion. In practice, an inner cannula can become permanently blocked with dried secretions beyond effective cleaning, cracked during removal, lost, or damaged during a clinical emergency. For patients on long-term tracheostomies (days to weeks in ICU, or months in home care), the original pair quickly needs supplementing. The 100/850 replacement pack ensures the bedside team always has a clean, genuine spare — avoiding the risk of prolonged use of a compromised or incompletely cleaned cannula.

Our patient is on a ventilator. Is the plain 100/850 the correct inner cannula, or should we use the fenestrated 100/851?

For any patient who is being mechanically ventilated, on CPAP, or who requires a fully sealed tracheal airway, the plain 100/850 is always the correct choice. The fenestrated 100/851 has openings in its wall — intentional for phonation and weaning — but these openings mean it cannot maintain a sealed airway circuit under positive pressure ventilation. Using a fenestrated inner cannula in a ventilated patient causes gas to leak out through the fenestrations rather than reaching the lungs, which is both ineffective and dangerous. The 100/851 is only appropriate when the patient is breathing independently and the clinical team has specifically prescribed fenestrated inner cannula use as part of a weaning or voice therapy plan.

A nurse accidentally used a 7.5 mm inner cannula (100/850/075) in a patient with a 7.0 mm outer tube. Is this dangerous?

Yes — this is a serious size mismatch and a potential patient safety incident. A larger inner cannula forced into a smaller outer tube will not seat correctly, will not click-lock properly, and may not be removable without significant force — particularly critical in an emergency when rapid decannulation or inner cannula removal is required. If a mismatch is suspected, the inner cannula must be removed immediately, the correct size confirmed from the outer tube flange markings, and the correct replacement inserted. All staff involved in tracheostomy care should be trained to verify size matching before every inner cannula insertion. Colour-coded packaging and size markings on each cannula are provided specifically to prevent this error.