Medical device discontinuation: Trutest arterial blood gas kit

The Trutest arterial blood gas kit 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 2025-02-05
Type of report Discontinuation
Discontinuation status To be discontinued
Name of medical deviceTable Footnote 2 if applicable Trutest arterial blood gas kit
Other names (for example, trade name), if applicable n/a
Package descriptionTable 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 T22151000 T22251000 T22251001 T22251020 T22253000 T22253010 T222532210 T222532310 T222532320 T222532320M T222535601
Medical device licence number (for Class II, III and IV), if known 107460
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

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