| Primary Device ID | B303B0100 |
| NIH Device Record Key | 553b7bfd-533c-4178-8a9f-65f589b1ce46 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MultiTech ULB |
| Version Model Number | MTULB |
| 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 | B303B0100 [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 | 2021-07-13 |
| Device Publish Date | 2021-07-05 |
| B303B0100 - MultiTech ULB | 2021-07-13 |
| B303B0100 - MultiTech ULB | 2021-07-13 |
| B303D0300 - VersaTech 1100 ULB | 2021-07-13 |
| B303E0200 - VersaTech 600 ULB | 2021-07-13 |
| B303F0100 - VersaTech LB | 2021-07-13 |
| B303A0000 - Multitech 2.0 | 2018-03-29 |
| B303B0000 - Multitech 8 | 2018-03-29 |
| B303C0000 - Varitech | 2018-03-29 |
| B303C0100 - Varitech 2.0 | 2018-03-29 |