| Primary Device ID | 05404028000632 |
| NIH Device Record Key | 95af1512-5eb8-49c3-91d8-04ac01cb6403 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Mimics Flow |
| Version Model Number | Mimics Flow |
| Catalog Number | Mimics Flow |
| Company DUNS | 373139427 |
| Company Name | Materialise NV |
| 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 | true |
| Serial Number | false |
| 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 | 05404028000632 [Primary] |
| OUG | Medical Device Data System |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-10-16 |
| Device Publish Date | 2023-10-06 |
| 05404028000762 - Mimics Cardiac Planner | 2024-10-24 Mimics Cardiac Planner |
| 05404028000816 - Materialise Mimics Enlight CMF | 2024-09-17 Mimics Enlight CMF Reconstruction Planner |
| 05420060367120 - AtlasPlan | 2024-07-29 Guide and Bone model for Reverse Shoulder Arthroplasty |
| 05404028000571 - Mimics Cardiac Planner | 2024-03-25 Mimics Cardiac Planner |
| 05420060367052 - AtlasPlan | 2023-12-27 Bone model for Reverse Shoulder Arthroplasty Aetos |
| 05420060367069 - AtlasPlan | 2023-12-27 Guide and Bone model for Reverse Shoulder Arthroplasty Aetos |
| 05420060367076 - AtlasPlan | 2023-12-27 Guide for Reverse Shoulder Arthroplasty Aetos |
| 05420060367083 - AtlasPlan | 2023-12-27 Guide and Bone model for Total Shoulder Arthroplasty Aetos |