Medical device discontinuation: Internal paddle electrodes
The Internal paddle electrode 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 | Date to be added by CPAB (YYYY-MM-DD) |
| Type of report | Discontinuation |
| Discontinuation status | Discontinued |
| Name of medical deviceTable Footnote 2 if applicable | Internal paddle electrodes |
| Other names (for example, trade name), if applicable | n/a |
| Package descriptionTable Footnote 3 | 1 Each |
| Class of medical device (I, II, III or IV), if known | II |
| Device identifier(s)Table Footnote 4 | 11131-000010 11131-000011 11131-000012 11131-000013 11131-000014 11131-000019 11131-000021 11131-000022 11131-000023 11131-000024 |
| Medical device licence number (for Class II, III and IV), if known | 103469 |
| Authorization identification number,Table Footnote 5 if applicable | n/a |
| Single-use product | No |
| Importers that have reported the discontinuation,Table Footnote 6 if applicable | Physio-Control Inc. |
| Manufacturer’s name | Physio-Control Inc. |
| Manufacturer’s mailing address | 11811 Willows Road North East, Redmond, WA, USA, 98052 |
| Reason for discontinuation | Manufacturing issues |
| Comments | n/a |