| Primary Device ID | 00802526488825 |
| NIH Device Record Key | d09c97ce-181d-4715-85af-509ae2224ef9 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 6032 |
| 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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00802526488825 [Primary] |
| DTB | permanent pacemaker Electrode |
| 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 |
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| 08714729784005 - Kinetix™ Plus | 2025-12-05 PTCA Guidewire |
| 08714729784029 - Kinetix™ Plus | 2025-12-05 PTCA Guidewire |
| 08714729784043 - Kinetix™ Plus | 2025-12-05 PTCA Guidewire |
| 08714729877479 - Dynamic Tip™ | 2025-12-03 Unidirectional Steerable Diagnostic Catheter |
| 08714729877486 - Dynamic Tip™ | 2025-12-03 Unidirectional Steerable Diagnostic Catheter |
| 08714729877493 - EP XT™ | 2025-12-03 Unidirectional Steerable Diagnostic Catheter |
| 08714729877509 - EP XT™ | 2025-12-03 Unidirectional Steerable Diagnostic Catheter |