| Primary Device ID | 00885914997581 |
| NIH Device Record Key | 7dc61b12-7371-4cd5-9df9-aac161335883 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DRY PAD |
| Version Model Number | 23" x 36" (58.4cm x 91.4cm), 10/PK |
| Company DUNS | 555240671 |
| Company Name | PHU BAO GROUP COMPANY LIMITED |
| Device Count | 10 |
| 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 | true |
| Lot Batch | true |
| Serial Number | true |
| 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 |