| Primary Device ID | 00816299012972 |
| NIH Device Record Key | d06d86a6-bb95-4a6e-bd2a-fc022fa4ac7c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HoverMatt PROS Air |
| Version Model Number | PROS2-HM-HC |
| Company DUNS | 942139841 |
| Company Name | Hovertech International |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Conditional |
| 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 | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00816299012965 [Primary] |
| GS1 | 00816299012972 [Package] Contains: 00816299012965 Package: Case [10 Units] In Commercial Distribution |
| FRZ | Device, Patient Transfer, 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 | 2026-03-09 |
| Device Publish Date | 2026-02-27 |
| 00816299012996 | The HoverMatt® PROS™ (Patient Repositioning Off-Loading System) Air, is breathable and used t |
| 00816299012972 | The HoverMatt® PROS™ (Patient Repositioning Off-Loading System) Air, is breathable and used t |
| 00816299012958 | The HoverMatt® PROS™ (Patient Repositioning Off-Loading System) Air, is breathable and used t |