| Primary Device ID | 00802526068034 |
| NIH Device Record Key | ac71c827-ca6b-439e-8cc0-e411eb6a7d76 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 6946 |
| Company DUNS | 106295384 |
| Company Name | BOSTON SCIENTIFIC CORPORATION |
| 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 | 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 | 00802526068034 [Primary] |
| LWS | Implantable cardioverter defibrillator (non-CRT) |
| 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 | 2014-09-24 |
| 08714729146841 - The Magnet™ | 2025-12-12 Exchange Device |
| 08714729008828 - The Magnet™ | 2025-12-12 Exchange Device |
| 08714729808497 - Flextome® Cutting Balloon® | 2025-12-12 Microsurgical Dilatation Device |
| 08714729808503 - Flextome® Cutting Balloon® | 2025-12-12 Microsurgical Dilatation Device |
| 08714729808510 - Flextome® Cutting Balloon® | 2025-12-12 Microsurgical Dilatation Device |
| 08714729808527 - Flextome® Cutting Balloon® | 2025-12-12 Microsurgical Dilatation Device |
| 08714729808534 - Flextome® Cutting Balloon® | 2025-12-12 Microsurgical Dilatation Device |
| 08714729808541 - Flextome® Cutting Balloon® | 2025-12-12 Microsurgical Dilatation Device |