| Primary Device ID | 00681490427296 |
| NIH Device Record Key | 0b7a4e94-651c-43f7-b590-97eab2aeeb04 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | TK2S24 |
| 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 | true |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00681490427296 [Primary] |
| CAC | APPARATUS, AUTOTRANSFUSION |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-06-17 |
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| 20199150032482 - NA | 2025-07-21 CUSTOM PACK 6S19R4 10PK DIALYSIS |
| 00199150033423 - NA | 2025-07-21 CUSTOM PACK BB12B90R7 SPECTRU |
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| 00199150033614 - NA | 2025-07-21 CUSTOM PACK BB10J74R14 3/8CNTRIS |
| 00199150034246 - NA | 2025-07-21 CUSTOM PACK BB11J86R12 ADULT E |
| 00763000925093 - FlexCath Cross™ Transseptal Solution | 2025-07-21 NDL 900302 FLEXCATH CROSS SL 63CM EIFU |