| 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  |