| Primary Device ID | M68980110130 |
| NIH Device Record Key | 6cba6759-5d5d-4985-94a7-9e9301763135 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SALINE LOCK KIT |
| Version Model Number | 13 |
| Catalog Number | 80-110 |
| Company DUNS | 118492643 |
| Company Name | Safeguard US Operating, 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 | true |
| 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 Issuing Agency | Device ID |
|---|---|
| HIBCC | M68980110130 [Primary] |
| LRS | I.V. Start Kit |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-12-20 |
| Device Publish Date | 2024-12-12 |
| M68980110120 | The Mojo® Saline Lock Kit allows for quick and effective extremity venous cannulation under the |
| M68980110130 | The Mojo® Saline Lock Kit allows for quick and effective extremity venous cannulation under the |
| M68980110140 | The Mojo® Saline Lock Kit allows for quick and effective extremity venous cannulation under the |
| M68980110110 | 18 GA. Catheter 1 ea 20 GA. Catheter 1 ea Saline Flush (5cc pre-filled s |