| Primary Device ID | 06934955979361 |
| NIH Device Record Key | 2871cef0-bf8f-4ed8-8b5e-e1232b1a7a30 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Sapphire ULTRA Coronary Dilatation Catheter |
| Version Model Number | 7932-010-11 |
| Company DUNS | 530923226 |
| Company Name | OrbusNeich Medical (ShenZhen) Co., Ltd. |
| 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 | false |
| OTC Over-The-Counter | false |