| Primary Device ID | 00802526488832 |
| NIH Device Record Key | 975302ee-b9c6-443c-a86e-23b75f872a60 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 6033 |
| 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 | 00802526488832 [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 |
| 08714729424260 - Contour™ | 2024-09-11 Ureteral Stent Set |
| 08714729462583 - Contour™ | 2024-09-11 Ureteral Stent Set |
| 08714729462651 - Contour™ | 2024-09-11 Ureteral Stent Set |
| 08714729462798 - Contour™ | 2024-09-11 Ureteral Stent Set |
| 00191506020798 - RHYTHMIA HDx™ | 2024-09-11 Ablation Connection Box - IntellaNav StablePoint™ (for INTELLAGEN™) |
| 00191506020804 - RHYTHMIA HDx™ | 2024-09-11 Ablation Connection Box (for INTELLAGEN™) |
| 08714729010975 - Connector | 2024-09-09 FOR 7F THROUGH 10F CATHETERS WITH LUER LOCK FITTING Ureteral Catheter Connector |
| 08714729010982 - Connector | 2024-09-09 FOR 3F THROUGH 6F CATHETERS WITH LUER LOCK FITTING Ureteral Catheter Connector |