| Primary Device ID | 00810113683720 |
| NIH Device Record Key | db13075e-39cd-4ef0-8143-be8a45682669 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Cold Compression Wrap, Pro-Knee Wrap-WL |
| Version Model Number | 401105 |
| Catalog Number | 401105 |
| Company DUNS | 084042331 |
| Company Name | Manamed, 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 | true |
| 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 |
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