Fusion1K

GUDID 00817365020310

FUSION CUSTOM SYSTEM

MOXI ENTERPRISES, LLC

Low-air-loss bed
Primary Device ID00817365020310
NIH Device Record Key0ca76e18-69ca-426f-888b-50eaad2b47dd
Commercial Distribution StatusIn Commercial Distribution
Brand NameFusion1K
Version Model NumberFUSCUST
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
GS100817365020310 [Primary]

FDA Product Code

FNMMattress, Air Flotation, Alternating Pressure

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 [Fusion1K]

00817365020310FUSION CUSTOM SYSTEM
00817365020228FUSION 1K SYSTEM 84" W/FR COVER
00817365020211FUSION 1K SYSTEM 84"
00817365020204FUSION 1K SYSTEM 80" w/visco heal
00817365020198FUSION 1K SYSTEM 80"

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