FUSXC80VIS1-4H

GUDID 00817365021157

FUSION XC 36X80 SYSTEM WITH HANDLES

MOXI ENTERPRISES, LLC

Orthopaedic bed mattress
Primary Device ID00817365021157
NIH Device Record Key38bc198c-4a8c-4624-ad13-bb8defa401a9
Commercial Distribution StatusIn Commercial Distribution
Brand NameFUSXC80VIS1-4H
Version Model NumberFUSXC80VIS1-4H
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
GS100817365021157 [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 Date2016-12-07

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