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.
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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