| Primary Device ID | 08714729479109 |
| NIH Device Record Key | a60b0065-eb53-472a-a162-e0fbba749e6e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | EZ Bent Tip |
| Version Model Number | H749501001500 |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 08714729479109 [Primary] |
| NFA | Temporary Coronary Saphenous Vein Bypass Graft for Embolic Protection |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-04-09 |
| Device Publish Date | 2016-09-24 |
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| 08714729877844 - Orbiter™ ST | 2024-12-20 Bidirectional Steerable Diagnostic Catheter |