| Primary Device ID | 00860036000524 |
| NIH Device Record Key | ae408330-40a9-4f5f-939c-788f10684ded |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Reprocessed Visions PV.018 Digital IVUS Catheter |
| Version Model Number | VEN-PV-018 |
| Catalog Number | VEN-PV-018 |
| 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 | 00860036000524 [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 | 2023-10-09 |
| Device Publish Date | 2023-09-29 |
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