| Primary Device ID | M6898011010040 |
| NIH Device Record Key | b6e7cd68-0aba-43cc-973e-52d3486f869e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 80-110-10 Saline Lock Kit Case of 10 |
| Version Model Number | 4 |
| Catalog Number | 80-110-10 |
| 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 |
| Phone | 1-855-428-6074 |
| sales@safeguardmedical.com | |
| Phone | 1-855-428-6074 |
| sales@safeguardmedical.com | |
| Phone | 1-855-428-6074 |
| sales@safeguardmedical.com | |
| Phone | 1-855-428-6074 |
| sales@safeguardmedical.com | |
| Phone | 1-855-428-6074 |
| sales@safeguardmedical.com | |
| Phone | 1-855-428-6074 |
| sales@safeguardmedical.com |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | M6898011010040 [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 | 2025-01-20 |
| Device Publish Date | 2025-01-11 |
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| M68980110130 - SALINE LOCK KIT | 2024-12-20 The Mojo® Saline Lock Kit allows for quick and effective extremity venous cannulation under the most demanding conditions in on |
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