| Primary Device ID | 00817012030525 |
| NIH Device Record Key | 0e537e15-7723-45c5-88aa-ee85e4b370c3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | K-Z iTURN |
| Version Model Number | K-9-PV-Z-AX-MS |
| Catalog Number | K-9-PV-Z-AX-MS |
| Company DUNS | 135241342 |
| Company Name | KAP MEDICAL |
| 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 |
| Phone | 951-340-4360 |
| sales@kapmedical.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00817012030525 [Primary] |
| IKZ | Bed, Patient Rotation, 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 | 2022-10-10 |
| Device Publish Date | 2022-09-30 |
| 00817012030174 | Alternating Rotation, Auto Immersion, Pulsation, True Low Air Loss, Percussion, Mattress System, |
| 00817012030167 | Alternating Rotation, Auto Immersion, Pulsation, True Low Air Loss, Percussion and Vibration, Ma |
| 00817012030525 | Percussion and Vibration, Auto Expansion, Touch Screen Display, Battery Backup, Alternating Pate |
| 00817012030518 | Percussion and Vibration, Auto Variable Length, Touch Screen Display, Battery Backup, Alternatin |
| 00817012031171 | Percussion and Vibration, Auto Expansion, Touch Screen Display, Auto Immersion / Auto Sensing, B |
| 00817012031164 | Percussion and Vibration, Auto Variable Length, Touch Screen Display, Auto Immserion / Auto Sens |