| Primary Device ID | 10884450681241 |
| NIH Device Record Key | 2714dc56-98df-4bef-84fd-31b7aaa33712 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Madison™ |
| Version Model Number | C |
| Catalog Number | KDPD1115 |
| Company DUNS | 184763290 |
| Company Name | Merit Medical Systems, Inc. |
| Device Count | 1 |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00884450681244 [Primary] |
| GS1 | 10884450681241 [Package] Contains: 00884450681244 Package: [10 Units] In Commercial Distribution |
| GAA | NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-07-21 |
| Device Publish Date | 2025-07-11 |
| 00884450393635 | 00884450393635 |
| 00884450393611 | 00884450393611 |
| 00884450393604 | 00884450393604 |
| 00884450393598 | 00884450393598 |
| 00884450393581 | 00884450393581 |
| 10884450411909 | 00884450411902 |
| 10884450411923 | 00884450411926 |
| 10884450411930 | 00884450411933 |
| 10884450411916 | 00884450411919 |
| 10884450411947 | 00884450411940 |
| 10884450681401 | C |
| 10884450681241 | C |
| 10884450681234 | C |
| 10884450681227 | C |
| 10884450681210 | C |