| Primary Device ID | G619450066091 |
| NIH Device Record Key | c49b3cd6-0016-4112-a529-754039c160ca |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | KBL |
| Version Model Number | BQ 607 Z4 F |
| Catalog Number | 45006609 |
| Company DUNS | 039280558 |
| Company Name | JW NORTH AMERICA, 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | true |