K-Z iTURN K-9-P-Z-MS

GUDID 00817012030174

Low-air-loss bed

Primary Device ID	00817012030174
NIH Device Record Key	4983d640-b19b-4801-b4db-ddb082c7260a
Commercial Distribution Status	In Commercial Distribution
Brand Name	K-Z iTURN
Version Model Number	K-9-P-Z-MS
Catalog Number	K-9-P-Z-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

Device Issuing Agency	Device ID
GS1	00817012030174 [Primary]

IKZ	Bed, Patient Rotation, Powered

Steralize Prior To Use	false
Device Is Sterile	false

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