| Primary Device ID | B303E040 |
| NIH Device Record Key | 408c295d-1f78-42a2-b812-1eb21524a1d2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VersaTech 700 ULB |
| Version Model Number | V7ULB+-xx-1000 |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B303E040 [Primary] |
| FNL | Bed, Ac-Powered Adjustable Hospital |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-04-21 |
| Device Publish Date | 2025-04-11 |
| B303D040 - VersaTech 1100 ULB | 2025-04-21 |
| B303D041 - VersaTech 1100 ULB+ | 2025-04-21 |
| B303D042 - VersaTech 1100 ULB+ | 2025-04-21 |
| B303E030 - VersaTech 600 ULB | 2025-04-21 |
| B303E031 - VersaTech 600 ULB+ | 2025-04-21 |
| B303E040 - VersaTech 700 ULB | 2025-04-21 |
| B303E040 - VersaTech 700 ULB | 2025-04-21 |
| B303E041 - VersaTech 700 ULB+ | 2025-04-21 |
| B303E042 - VersaTech 700 ULB+ | 2025-04-21 |