| Primary Device ID | 00814384020352 |
| NIH Device Record Key | 2f957c44-910d-47c3-8dce-1506ba7cc22e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Galeo Pro |
| Version Model Number | 300 CM |
| Catalog Number | 389791 |
| Company DUNS | 189689800 |
| Company Name | CONCERT MEDICAL, LLC |
| Device Count | 5 |
| 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 |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 104 Degrees Fahrenheit |
| Storage Environment Temperature | Between 50 Degrees Fahrenheit and 104 Degrees Fahrenheit |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00814384020345 [Unit of Use] |
| GS1 | 00814384020352 [Primary] |
| DQX | Wire, Guide, Catheter |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-26 |
| 00814384020352 | Coronary Guidewire |
| 00814384020338 | Coronary Guidewire |
| 00814384020314 | Coronary Guidewire |
| 00814384020291 | Coronary Guidewire |
| 00814384020277 | Coronary Guidewire |
| 00814384020253 | Coronary Guidewire |
| 00814384020239 | Coronary Guidewire |
| 00814384020215 | Coronary Guidewire |
| 00814384020192 | Coronary Guidewire |