| Primary Device ID | 00810055880836 |
| NIH Device Record Key | 0212ab27-a287-423c-b94a-a1a7dd1506cf |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ProMatt Plus |
| Version Model Number | PMP-ES |
| Company DUNS | 790937150 |
| Company Name | JOERNS HEALTHCARE, LLC |
| Device Count | 1 |
| DM Exempt | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810055880836 [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 | 2023-08-22 |
| Device Publish Date | 2023-08-14 |
| 00857268006660 | PMP-CBC |
| 00810055880461 | PRO TECHNOLOGY PUMP - AU/NZ |
| 00810055880454 | PRO TECHNOLOGY PUMP - EU |
| 00810055880447 | PRO TECHNOLOGY PUMP - UK |
| 00810055880430 | PRO TECHNOLOGY PUMP - US/CA |
| 00810055880904 | CONTROL UNIT, PROMATT ATA, UK |
| 00810055880898 | PROMATT PLUS 90CM MATTRESS DURATUB |
| 00810055880881 | PROMATT PLUS 85CM X 215CM DURATUB |
| 00810055880874 | PROMATT PLUS 85cm MATTRESS DURATUB |
| 00810055880867 | PROMATT PLUS 78CM MATTRESS DURATUB |
| 00810055880850 | PWR UNIT, PROMATT ES AUTO FIRM TO ALT EU |
| 00810055880843 | PROMATT PLUS 90X200 MATTRESS, NYLON |
| 00810055880836 | PREMIUM ES PROMATT |
| 00810055884377 | PROMATT PLUS 85CM X 210CM DURATUB |