| Primary Device ID | 10688503001051 |
| NIH Device Record Key | 562cea4e-51ec-4d5d-a12d-b20dc9a6cbe7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Savaria |
| Version Model Number | M921780 |
| Catalog Number | M921780 |
| Company DUNS | 208913722 |
| Company Name | Savaria Concord Lift |
| 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 |
|---|---|
| GS1 | 10688503001051 [Primary] |
| FRW | Scale, Patient |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-06-06 |
| Device Publish Date | 2025-05-29 |
| 10688503001068 | Scale Carry Bar |
| 10688503001051 | Scale Carry Bar |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SAVARIA 77960467 4184685 Live/Registered |
Savaria Concord Lifts Inc. 2010-03-16 |