| Primary Device ID | 10673978522248 |
| NIH Device Record Key | cf1c6c69-fe3f-40b1-96f5-30979dd8d822 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | BT133 |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00673978522241 [Primary] |
| GS1 | 10673978522248 [Package] Contains: 00673978522241 Package: PK [10 Units] In Commercial Distribution |
| 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 |
| 00199150031610 - NA | 2025-07-21 CUSTOM PACK BB1U06R24 CHRIS AD |
| 00199150032464 - NA | 2025-07-21 CUSTOM PACK BB10R35R4 CP PRIME |
| 20199150032482 - NA | 2025-07-21 CUSTOM PACK 6S19R4 10PK DIALYSIS |
| 00199150033423 - NA | 2025-07-21 CUSTOM PACK BB12B90R7 SPECTRU |
| 20199150033571 - NA | 2025-07-21 CUSTOM PACK BB2U59R3 2PK 1/4 TBL L |
| 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 |