| Primary Device ID | 04260735022425 |
| NIH Device Record Key | a2043962-d70e-4327-b276-05b629cc3735 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Carlo Classic Alu Patient Lift |
| Version Model Number | 924003018 |
| Company DUNS | 342212273 |
| Company Name | BEKA Hospitec 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 | false |
| 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 | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04260735022425 [Primary] |
| FSA | Lift, Patient, Non-Ac-Powered |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-04-08 |
| Device Publish Date | 2025-03-31 |
| 04260735022425 | Carlo Classic Alu Patient Lift |
| 04260735022418 | Carlo Classic ALU Patient Lift |
| 04260735022401 | Carlo Classic Alu Patient Lift |
| 04260735020636 | Carlo Classic ALU Patient Lift |
| 04260735020629 | Carlo Classic ALU Patient Lift |
| 04260735020605 | Carlo Classic ALU Patient Lift |
| 04260735020506 | Carlo Classic ALU Patient Lift |
| 04260735020490 | Carlo Classic ALU Patient Lift |