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Medical device discontinuation: Silicone ventilation tube - silverstein spat

The Silicone ventilation tube - silverstein spat is currently reported as a medical device discontinuation under sections 62.21 to 62.26 of the Medical Devices Regulations. For a full list of shortages, refer to the list of shortages and discontinuations.

Details of the medical device discontinuation report
Report information Details
Posted dateTable Footnote 1 2025-04-10
Type of report Discontinuation
Discontinuation status Discontinued
Name of medical deviceTable Footnote 2 if applicable Silicone ventilation tube - silverstein spat
Other names (for example, trade name), if applicable n/a
Package descriptionTable Footnote 3 5 pack
Class of medical device (I, II, III or IV), if known III
Device identifier(s)Table Footnote 4 1028065
Medical device licence number (for Class II, III and IV), if known 14550
Authorization identification number,Table Footnote 5 if applicable n/a
Single-use product Yes
Importers that have reported the discontinuation,Table Footnote 6 if applicable n/a
Manufacturer's name Medtronic Xomed Inc.
Manufacturer's mailing address 6743 Southpoint Drive North
Jacksonville, Florida, 32216, Usa
Reason for discontinuation Business reasons
Comments n/a

Table footnotes

Table Footnote 1

This date reflects when a discontinuation report is first posted online. This page includes specific information about the device that is in shortage

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Table Footnote 2

Including any component, accessory, consumable material or part that is in shortage, including the model name

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Table Footnote 3

For example, packaging formats, sizes, quantities

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Table Footnote 4

For example, serial number, catalogue number, part number, model number or unique device identifier

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Table Footnote 5

The authorization identification number is specific to the medical device's authorization (for example, medical device licence number, interim order authorization number)

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Table Footnote 6

Names of importers listed who have reported the discontinuation separately from the manufacturer or who are reporting on behalf of the manufacturer in a delegated capacity

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