Medical device discontinuation: Arterial blood gas kit(s)

The Arterial blood gas kit(s) 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 date^{Table Footnote 1}	2025-02-05
Type of report	Discontinuation
Discontinuation status	To be discontinued
Name of medical device^{Table Footnote 2} if applicable	Arterial blood gas kit(s)
Other names (for example, trade name), if applicable	n/a
Package description^{Table Footnote 3}	Single-use medical devices (packaged in sterile peel-packs), sold in cases of 100/ea
Class of medical device (I, II, III or IV), if known	II
Device identifier(s)^{Table Footnote 4}	M023400MU M024023EC10106 M024023RHEC M029025TRUMU M02P4023LTRUBPMU M02P4023LTRUMU M02P9000RHST M02PT4522RHSL
Medical device licence number (for Class II, III and IV), if known	61583
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	Trudell Healthcare Solutions Inc.
Manufacturer’s mailing address	758 Baransway Drive London, Ontario, N5V 5J7, Canada
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 Return to table footnote 1 referrer Table Footnote 2 Including any component, accessory, consumable material or part that is in shortage, including the model name Return to table footnote 2 referrer Table Footnote 3 For example, packaging formats, sizes, quantities Return to table footnote 3 referrer Table Footnote 4 For example, serial number, catalogue number, part number, model number or unique device identifier Return to table footnote 4 referrer 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) Return to table footnote 5 referrer 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 Return to table footnote 6 referrer

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Date modified:: 2025-02-05