| Primary Device ID | 20763000558295 |
| NIH Device Record Key | a59bfcb8-3613-4b67-8562-8a224085ab85 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RACT |
| Version Model Number | 402-02 |
| Company DUNS | 006261481 |
| Company Name | MEDTRONIC, 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00763000558291 [Primary] |
| GS1 | 20763000558295 [Package] Contains: 00763000558291 Package: PK [15 Units] In Commercial Distribution |
| JPA | SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2026-03-02 |
| Device Publish Date | 2026-02-22 |
| 20643169577484 | CARTRIDGE 402-02 ACT RACT 13 LAN |
| 20613994531821 | CARTRIDGE 402-02 ACT RACT 14L |
| 20613994417286 | CARTRIDGE 402-02 ACT RACT 13 LAN |
| 00763000433833 | CARTRIDGE 402-02 ACT RACT 13 LAN |
| 20763000558295 | CARTRIDGE 402-02 ACT RACT 17 LAN |