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.
| 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 | Arterial blood gas kit(s) |
| 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 | 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 |