| Primary Device ID | 00836559006916 |
| NIH Device Record Key | daea1892-b87e-4364-b90d-1ae332c9cf24 |
| Commercial Distribution Discontinuation | 2017-10-27 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Venos Occlusion Balloon Catheter |
| Version Model Number | V0510010 |
| Catalog Number | V0510010 |
| Company DUNS | 101835833 |
| Company Name | Oscor Inc. |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(727)937-2511 |
| sales@oscor.com |
| Device Size Text, specify | 0 |
| Storage Environment Temperature | Between 5 Degrees Celsius and 30 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00836559006916 [Primary] |
| DYG | CATHETER, FLOW DIRECTED |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[00836559006916]
Ethylene Oxide
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2017-11-30 |
| 00836559007111 | Occlusion Balloon Catheter, 6F |
| 00836559007104 | Occlusion Balloon Catheter, 6F |
| 00836559007098 | Occlusion Balloon Catheter, 6F |
| 00836559007081 | Occlusion Balloon Catheter, 5F |
| 00836559007074 | Occlusion Balloon Catheter, 5F |
| 00836559006930 | Occlusion Balloon Catheter, 6F |
| 00836559006923 | Occlusion Balloon Catheter, 6F |
| 00836559006916 | Occlusion Balloon Catheter, 5F |
| 00836559006909 | Occlusion Balloon Catheter, 5F |