| Primary Device ID | 30815614020792 |
| NIH Device Record Key | bb36898b-a442-40b1-8657-425f27355741 |
| Commercial Distribution Discontinuation | 2023-06-30 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Cordis Zephyr Vascular Compression Band |
| Version Model Number | 190102 |
| Company DUNS | 042075700 |
| Company Name | SEMLER TECHNOLOGIES, 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 | false |
| 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 | 10815614020798 [Primary] |
| GS1 | 20815614020795 [Package] Contains: 10815614020798 Package: Box [5 Units] Discontinued: 2023-06-30 Not in Commercial Distribution |
| GS1 | 30815614020792 [Package] Contains: 20815614020795 Package: Carton [10 Units] Discontinued: 2023-06-30 Not in Commercial Distribution |
| DXC | Clamp, Vascular |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2023-07-03 |
| Device Publish Date | 2018-10-15 |
| 20815614020870 | The Cordis Zephyr Vascular Compression Band Model 190102 has a single inflatable compression bal |
| 20815614020863 | The Cordis Zephyr Vascular Compression Band Model 190101 has a single inflatable compression bal |
| 30815614020792 | The Cordis Zephyr Vascular Compression Band Model 190102 has a single inflatable compression bal |
| 30815614020785 | The Cordis Zephyr Vascular Compression Band Model 190101 has a single inflatable compression bal |