| Primary Device ID | 00860036000593 |
| NIH Device Record Key | 5adf2f53-adef-47bb-b7b9-a46770eed767 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Vein360 Reprocessed Eagle Eye Platinum ST Rx Digital IVUS Catheter |
| Version Model Number | VEN-PV-EEPST |
| Catalog Number | VEN-PV-EEPST |
| Company DUNS | 080926907 |
| Company Name | Vein360 LLC |
| 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 | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860036000593 [Primary] |
| OWQ | Reprocessed Intravascular Ultrasound Catheter |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-04-02 |
| Device Publish Date | 2024-03-25 |
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