| Primary Device ID | 07613365501070 |
| NIH Device Record Key | feb0ef53-3be1-41fe-9465-a9771e9d5352 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PowerCube+ Series |
| Version Model Number | A |
| Company DUNS | 318498177 |
| Company Name | Ganshorn Medizin Electronic GmbH |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613365501070 [Primary] |
| JEH | Plethysmograph, Volume |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-12-30 |
| Device Publish Date | 2024-12-20 |
| 07613365501094 | The PowerCube Body+ / Diffusion+ include a standard body plethysmography chamber with a door tha |
| 07613365501070 | The PowerCube Body+ / Diffusion+ include a standard body plethysmography chamber with a door tha |
| 07613365501032 | The PowerCube Body+ include a standard body plethysmography chamber with a door that opens to th |
| 07613365501018 | The PowerCube Body+ include a standard Body Plethmography chamber with a door that opens to the |
| 07613365500431 | The PowerCube Body+ and Diffusion+ include an extra-large body plethysmography chamber. |
| 07613365500400 | The PowerCube Body+ and Diffusion+ include a wheelchair-accessible body plethysmography chamber. |
| 07613365500301 | The PowerCube Diffusion+ is equipped with the MultiX Trolley. |