| Primary Device ID | B303D042 |
| NIH Device Record Key | 4bbe1ae4-4a49-4304-a5d5-8de3ce7cf41e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VersaTech 1100 ULB+ |
| Version Model Number | V11ULB+-xx-1110 |
| Company DUNS | 245707815 |
| Company Name | Usine Rotec Inc |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |