| Primary Device ID | 00817365020372 |
| NIH Device Record Key | 4fa2704a-3154-4ebd-b499-26e3e36c2af8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FusionXC |
| Version Model Number | FUSXCCUST |
| Company DUNS | 958807575 |
| Company Name | MOXI ENTERPRISES, LLC |
| 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 | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00817365020372 [Primary] |
| IKY | Mattress, Flotation Therapy, Non-Powered |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-08-11 |
| 00817365021171 | FUSION XC SYSTEM 39 x 80 |
| 00817365020402 | MEDLINE FUSION PLUS MATTRESS W/VISCO HEEL SECTION, 80" |
| 00817365020396 | MEDLINE FUSION PLUS MATTRESS W/VISCO HEEL SECTION, 84" |
| 00817365020389 | MEDLINE FUSION PLUS MATTRESS W/VISCO HEEL SECTION, 80" |
| 00817365020372 | FUSION XC SYSTEM, CUSTOM SIZE |
| 00817365020365 | FUSION XC SYSTEM 84" |
| 00817365020358 | FUSION XC SYSTEM 80" W/VISCO HEEL & 1" VISCO TOP |
| 00817365020341 | FUSION XC SYSTEM 80" |
| 00817365020334 | FUSION XC SYSTEM 36" x 77" |