| Primary Device ID | 00670482000722 |
| NIH Device Record Key | c6ef060c-834a-46f2-a20e-d1787a4b816c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Transport shelf |
| Version Model Number | 299-0523WG-TRI |
| Company DUNS | 249675476 |
| Company Name | Umano Medical 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 | true |
| Serial Number | false |
| 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 | 00670482000722 [Primary] |
| GS1 | 10670482000729 [Package] Package: [1 Units] In Commercial Distribution |
| 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 | 2023-12-13 |
| Device Publish Date | 2023-12-05 |
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