| Primary Device ID | 07613327424140 |
| NIH Device Record Key | 0c04f0e7-f0b0-4c8b-829e-bd10d2894e83 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ProForm |
| Version Model Number | 2815 |
| Catalog Number | 281505550005 |
| Company DUNS | 078470558 |
| Company Name | STRYKER CORPORATION |
| 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 | false |
| 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 | false |
| Handling Environment Temperature | Between -40 Degrees Celsius and 60 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327424140 [Primary] |
| IKY | MATTRESS, FLOTATION THERAPY, NON-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 | 2019-05-28 |
| Device Publish Date | 2019-05-20 |
| 07613327424164 | 2815 |
| 07613327424133 | 2815 |
| 07613327424157 | 2815 |
| 07613327424140 | 2815 |
| 07613327424119 | 2815 |
| 07613327424102 | 2815 |
| 07613327424065 | 2815 |
| 07613327485813 | 2815 |