FusionXC

GUDID 00817365020372

FUSION XC SYSTEM, CUSTOM SIZE

MOXI ENTERPRISES, LLC

Orthopaedic bed mattress
Primary Device ID00817365020372
NIH Device Record Key4fa2704a-3154-4ebd-b499-26e3e36c2af8
Commercial Distribution StatusIn Commercial Distribution
Brand NameFusionXC
Version Model NumberFUSXCCUST
Company DUNS958807575
Company NameMOXI ENTERPRISES, LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100817365020372 [Primary]

FDA Product Code

IKYMattress, Flotation Therapy, Non-Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-08-11

On-Brand Devices [FusionXC]

00817365021171FUSION XC SYSTEM 39 x 80
00817365020402MEDLINE FUSION PLUS MATTRESS W/VISCO HEEL SECTION, 80"
00817365020396MEDLINE FUSION PLUS MATTRESS W/VISCO HEEL SECTION, 84"
00817365020389MEDLINE FUSION PLUS MATTRESS W/VISCO HEEL SECTION, 80"
00817365020372FUSION XC SYSTEM, CUSTOM SIZE
00817365020365FUSION XC SYSTEM 84"
00817365020358FUSION XC SYSTEM 80" W/VISCO HEEL & 1" VISCO TOP
00817365020341FUSION XC SYSTEM 80"
00817365020334FUSION XC SYSTEM 36" x 77"

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