| Primary Device ID | 00887868551994 |
| NIH Device Record Key | f15fdf8c-2de6-48b3-9b55-0514fffec464 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | mymobility Platform- Patient Web Experience |
| Version Model Number | MMPWE001 |
| Catalog Number | MMPWE001 |
| Company DUNS | 117672130 |
| Company Name | Zimmer Us, 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 | true |
| Serial Number | false |
| 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 | 00887868551994 [Primary] |
| KQW | Goniometer, Nonpowered |
| KQX | Goniometer, Ac-Powered |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-02-11 |
| Device Publish Date | 2022-02-03 |
| 00889024680708 - mymobility® Platform | 2024-11-13 |
| 00889024680739 - mymobility® Platform | 2024-11-13 |
| 00889024680746 - mymobility® Platform | 2024-11-13 |
| 00889024680753 - mymobility® Platform | 2024-11-13 |
| 00887868581120 - mymobility® Platform | 2023-09-15 |
| 00887868581151 - mymobility® Platform | 2023-09-15 |
| 00887868581168 - mymobility® Platform | 2023-09-15 |
| 00887868581175 - mymobility® Platform | 2023-09-15 |