| Primary Device ID | 00822383551067 |
| NIH Device Record Key | b63797c8-5683-4949-925e-a0fe52d8fb21 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | WCF |
| Version Model Number | KG 1800BK WCF |
| Company DUNS | 867673159 |
| Company Name | Drive Devilbiss Healthcare |
| 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 | false |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | true |