| Primary Device ID | 00643169615984 |
| NIH Device Record Key | 4dcaa3b3-cfa6-4f89-be0a-66905d84e2c8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Symplicity G3™ |
| Version Model Number | RDN019 |
| Company DUNS | 006261481 |
| Company Name | MEDTRONIC, 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 | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00643169615984 [Primary] |
| BZN | CART, EMERGENCY, CARDIOPULMONARY (EXCLUDING EQUIPMENT) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-04-25 |
| Device Publish Date | 2017-04-23 |
| 00643169615984 | SYMPLICITY RDN019 G3 CART GLOBAL |
| 00763000387037 | CART RDN019 SYMPLICITY G3 GLOBAL |
| 00763000387020 | GENERATOR RDNG3A G3SV5.1 US JP CA |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SYMPLICITY G3 85711216 4951592 Live/Registered |
Medtronic Ardian Luxembourg S.a.r.l. 2012-08-23 |