Fusion DF

GUDID 00817365021156

FUSION 42x80x8 Mattress with Dry Floatation Insert

MOXI ENTERPRISES, LLC

Orthopaedic bed mattress
Primary Device ID00817365021156
NIH Device Record Keya05a801e-1c19-41e7-8761-87f3eed21bce
Commercial Distribution StatusIn Commercial Distribution
Brand NameFusion DF
Version Model NumberFUSXL4280DF
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
GS100817365021156 [Primary]

FDA Product Code

IKYMattress, Flotation Therapy, Non-Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-07-26
Device Publish Date2018-06-25

On-Brand Devices [Fusion DF]

00817365021156FUSION 42x80x8 Mattress with Dry Floatation Insert
00817365021676FUSION 42x80x8 Mattress with Dry Floatation Insert

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