Primary Device ID | 00817012030600 |
NIH Device Record Key | 2e8d800b-0ee0-4f59-b535-435bdff0ca2d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | K-4IM IntelliMatt |
Version Model Number | K-4-IM-AVL-MS |
Catalog Number | K-4-IM-AVL-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 | 00817012030600 [Primary] |
FNM | Mattress, Air Flotation, Alternating Pressure |
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 |
00817012030624 | Alternating Pressure, Auto Immersion, Pulsating, Low Air Loss, Auto Expansion, Mattress System, |
00817012030617 | Alternating Pressure, Auto Immersion, Pulsating, Low Air Loss, Auto Variable Length, Mattress Sy |
00817012030600 | Alternating Pressure, Auto Immersion, Pulsating, Low Air Los, Auto Variable Length, Mattress Sys |