| Primary Device ID | 00817369021818 |
| NIH Device Record Key | 7fc35b74-6e64-4d9d-8fce-4795ebb53d20 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NormaTec MVP Pro Upper and Lower Body Recovery Package |
| Version Model Number | MVP Pro Recovery Package - Upper and Lower Body Po |
| Catalog Number | 40435 |
| Company DUNS | 111448069 |
| Company Name | NORMATEC INDUSTRIES LP |
| 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 | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00817369021818 [Primary] |
| JOW | Sleeve, Limb, Compressible |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-14 |
| 00817369021818 | MVP Pro Recovery Package - Upper and Lower Body Power Tall |
| 00817369021801 | MVP Pro Recovery Package - Upper and Lower Body Power Standard |
| 00817369021795 | MVP Pro Recovery Package - Upper and Lower Body Power Short |
| 00817369021788 | MVP Pro Recovery Package - Upper and Lower Body Short |
| 00817369021771 | MVP Pro Recovery Package - Upper and Lower Body Tall |
| 00817369021764 | MVP Pro Recovery Package - Upper and Lower Body Standard |