| Primary Device ID | 08714729877509 |
| NIH Device Record Key | d82d0e57-c993-42ad-a37c-849c5d8009fd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | EP XT™ |
| Version Model Number | M0042007700 |
| Catalog Number | M0042007700 |
| Company DUNS | 021717889 |
| 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 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 | 08714729877509 [Primary] |
| DRF | CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2025-12-03 |
| Device Publish Date | 2016-09-24 |
| 08714729877592 | Unidirectional Steerable Diagnostic Catheter |
| 08714729877578 | Unidirectional Steerable Diagnostic Catheter |
| 08714729877561 | Unidirectional Steerable Diagnostic Catheter |
| 08714729877554 | Unidirectional Steerable Diagnostic Catheter |
| 08714729877547 | Unidirectional Steerable Diagnostic Catheter |
| 08714729877509 | Unidirectional Steerable Diagnostic Catheter |
| 08714729877493 | Unidirectional Steerable Diagnostic Catheter |