| Primary Device ID | 10816513023859 |
| NIH Device Record Key | 74ada4b4-c339-47f6-a084-d9f500bde5a1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Set Administration Intravascular |
| Version Model Number | KMI-CL-LLP |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00816513023852 [Primary] |
| GS1 | 10816513023859 [Package] Contains: 00816513023852 Package: BOX [100 Units] In Commercial Distribution |
| FPA | Set, Administration, Intravascular |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-07-03 |
| Device Publish Date | 2019-06-25 |
| 00816513022602 | SM-007 |
| 00816513022596 | NP-003 |
| 00816513022589 | HR-015-BS |
| 00816513022572 | FL1002-FM |
| 00816513022565 | EG-016-05 |
| 00816513022541 | EB-038-12 |
| 00816513022510 | DD-001-28 |
| 00816513022497 | DB-008-04 |
| 10816513023958 | BGI-BC105 |
| 10816513023859 | KMI-CL-LLP |
| 10816513024863 | DB-009-01 |