| Primary Device ID | 04260647946352 |
| NIH Device Record Key | ad3c5169-264c-4261-93b4-43d7b9687cc0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AKRUS |
| Version Model Number | AK480 |
| Company DUNS | 324099522 |
| Company Name | AKRUS GmbH & Co. KG |
| 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 | 04260647946352 [Primary] |
| FZM | Stool, Operating-Room |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-12-19 |
| Device Publish Date | 2023-12-11 |
| 04260647940008 | CZM IT760.i |
| 04260647946239 | AK 106 |
| 04260647943573 | Patient Support System LSCneo |
| 04260647941562 | SC 5010SEK |
| 04260647941517 | AK 5010MBS |
| 04260647940015 | CZM IT1060.i |
| 04260647946352 | AK480 |
| 04260647945744 | AK 447 |
| 04260647945706 | AK446 |
| 04260647945560 | Doctor Stool ak 445 |
| 04260647945539 | Doctor stool ak 445 |
| 04260647945515 | AK 445 |