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 |