| Primary Device ID | 00815212020278 |
| NIH Device Record Key | 3b522625-8395-40cf-bd61-9f33364f1e75 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Multi-Modality Markers |
| Version Model Number | 52160 |
| Company DUNS | 933506164 |
| Company Name | Izi Medical Products, LLC |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| 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 | 00815212020278 [Primary] |
| IYE | Accelerator, Linear, Medical |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2017-01-25 |
| 00815212022869 | S-MM3005 |
| 00815212022845 | S-MM3002 |
| 00815212022784 | MM3005-VIP |
| 00815212022777 | MM3005CLM |
| 00815212022753 | REG3002 |
| 00815212020773 | MM3007 |
| 00815212020766 | MM3005 |
| 00815212020759 | MM3003 |
| 00815212020742 | MM3002-60 |
| 00815212020735 | MM3002-10I |
| 00815212020728 | MM3002-100 |
| 00815212020711 | MM3002-10 |
| 00815212020704 | MM3002 |
| 00815212020278 | 52160 |
| 00815212020261 | 960-991 |
| 10815212020268 | 960-991 |