| Primary Device ID | 00816513022206 |
| NIH Device Record Key | f94d70ce-ac9a-4b23-8686-84236ff8965d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Set, Administration, Intravascular |
| Version Model Number | S-100-29 |
| Company DUNS | 079636164 |
| Company Name | MPS MEDICAL, INC |
| 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 | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |