| Primary Device ID | 04050621100012 |
| NIH Device Record Key | a28a891e-023f-4cc2-b757-5ff2b107eb54 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | sentida 03 |
| Version Model Number | 19-1062 |
| Company DUNS | 340866990 |
| Company Name | WISSNER-BOSSERHOFF GmbH |
| 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 | 04050621100012 [Primary] |
| LLI | Bed, Therapeutic, Ac-Powered, Adjustable Home-Use |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-11-18 |
| Device Publish Date | 2019-11-08 |
| 04050621100555 - sentida 5 xxl | 2024-09-06 |
| 04050621100609 - sentida sc-xl USA | 2024-09-06 |
| 04050621100616 - sentida sc-xxl USA | 2024-09-06 |
| 04050621100593 - sentida sc USA | 2023-09-21 |
| 04050621100432 - sentida 04 | 2023-01-12 Basic electric home bed |
| 04050621100463 - sentida 6-xl | 2023-01-12 Basic electric home bed |
| 04050621100470 - sentida 5-le | 2023-01-12 |
| 04050621100487 - sentida 6-le | 2023-01-12 Basic electric home bed |