| Primary Device ID | 00884450828748 |
| NIH Device Record Key | 7ff096fb-13e7-4950-949b-9eba8c57b173 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SAFEGUARD FOCUS™ |
| Version Model Number | B |
| Catalog Number | SGF1A |
| Company DUNS | 184763290 |
| Company Name | Merit Medical Systems, Inc. |
| Device Count | 5 |
| 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 | 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 | true |
| OTC Over-The-Counter | false |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00884450828748 [Unit of Use] |
| GS1 | 10884450828745 [Primary] |
| MHW | Dressing, compression |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-01-09 |
| Device Publish Date | 2025-01-01 |
| 00884450524763 | 10884450524760 |
| 00884450524770 | 10884450524777 |
| 00884450828748 | B |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SAFEGUARD FOCUS 90651859 not registered Live/Pending |
Merit Medical Systems, Inc. 2021-04-16 |