| Primary Device ID | 04046768149564 |
| NIH Device Record Key | d04176f5-0b1a-4ded-a0db-fab09a8f2ff7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | pair of leg plates |
| Version Model Number | 111861FC |
| Company DUNS | 315435859 |
| Company Name | MAQUET 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 | 04046768149564 [Primary] |
| BWN | Table And Attachments, 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 | 2024-04-19 |
| Device Publish Date | 2024-04-11 |
| 04046768138353 | 116050DC |
| 04046768137738 | 116050GC |
| 04046768137721 | 116050BC |
| 04046768134669 | 116050FC |
| 04046768134652 | 116050AC |
| 04046768133303 | 100742AC |
| 04046768103153 | 115064E0 |
| 04046768075849 | 115073DC |
| 04046768073807 | 115073BC |
| 04046768073296 | 113373BC |
| 04046768073036 | 113373FC |
| 04046768040977 | 118054G0 |
| 04046768032033 | 118054F0 |
| 04046768032026 | 118054B0 |
| 04046768032002 | 118054A0 |
| 04046768031203 | 115064B0 |
| 04046768030183 | 111850F0 |
| 04046768003637 | 115064D0 |
| 04046768002982 | 113353FC |
| 04046768002975 | 113353BC |
| 04046768002395 | 111850B0 |
| 04046768149564 | 111861FC |
| 04046768149557 | 111861BC |