| Primary Device ID | 00802526489013 |
| NIH Device Record Key | e32efe36-24ec-49a1-a2b8-78df9b0eb221 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 6052 |
| 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 | 00802526489013 [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 |
| 08714729011378 - Lubriglide | 2024-12-23 Coated Guidewire |
| 08714729011392 - Lubriglide | 2024-12-23 Coated Guidewire |
| 08714729012580 - Lubriglide | 2024-12-23 Coated Guidewire |
| 08714729012603 - Lubriglide | 2024-12-23 Coated Guidewire |
| 08714729012610 - Lubriglide | 2024-12-23 Coated Guidewire |
| 08714729056645 - Lubriglide | 2024-12-23 Coated Guidewire |
| 08714729057062 - Lubriglide | 2024-12-23 Coated Guidewire |
| 08714729080602 - MaxForce TTS | 2024-12-23 High Performance Balloon Dilatation Catheter |