| Primary Device ID | 05060493790005 |
| NIH Device Record Key | 649ac7a2-2408-40c5-9a4b-3578eb8e1345 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Beds by George |
| Version Model Number | 180 |
| Company DUNS | 054233501 |
| Company Name | BEDS BY GEORGE |
| 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 | 05060493790005 [Primary] |
| FNL | Bed, Ac-Powered Adjustable Hospital |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-08 |
| 05060493790111 | 36x80 semi-electric |
| 05060493790104 | 36x80 semi-electric |
| 05060493790098 | 36x80 semi-electric |
| 05060493790081 | 36x80 semi-electric |
| 05060493790074 | 36x80 |
| 05060493790067 | 36x76 |
| 05060493790050 | 36x80 |
| 05060493790043 | 36x76 |
| 05060493790036 | 36x80 |
| 05060493790029 | 36x76 |
| 05060493790012 | 36x80 |
| 05060493790005 | 36x76 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() BEDS BY GEORGE 77390014 3504446 Live/Registered |
Beds By George, Inc. 2008-02-06 |