| Primary Device ID | G434DRY320 |
| NIH Device Record Key | ad376e23-da78-42c2-9a19-7253bcb6caa8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DRY320 |
| Version Model Number | DRY320 |
| Company DUNS | 118762097 |
| Company Name | Wassenburg Medical, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | DRY320 [Primary] |
| HIBCC | G434DRY320 [Package] Contains: DRY320 Package: corrugated box [1 Units] In Commercial Distribution |
| JRJ | Unit, Drying |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-11-08 |
| Device Publish Date | 2023-10-31 |
| G434DRY320 | A device to store and dry endoscopes |
| 00860010835234 | A device to store and dry endoscopes |