| Primary Device ID | 10816765013073 |
| NIH Device Record Key | 0802e877-cdda-41ea-8487-7714e98d48dd |
| Commercial Distribution Discontinuation | 2020-03-31 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Version Model Number | 710426 |
| Catalog Number | 710426 |
| Company DUNS | 202659140 |
| Company Name | Corporation Steris Canada |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
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