Fusion 2K

GUDID 00817365020304

Fusion 2K XL 42x80x8

MOXI ENTERPRISES, LLC

Low-air-loss bed
Primary Device ID00817365020304
NIH Device Record Key2c80fe18-8bd2-4160-893b-d322d265a608
Commercial Distribution StatusIn Commercial Distribution
Brand NameFusion 2K
Version Model NumberFUS2KXL4280
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
GS100817365020304 [Primary]

FDA Product Code

FNMMattress, Air Flotation, Alternating Pressure

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-06-07
Device Publish Date2018-05-07

On-Brand Devices [Fusion 2K]

00817365021607Fusion 2K XL 48x80x8
00817365020306Fusion 2K XL 48x80x8 Canada
00817365020305Fusion 2K XL 42x80x8 Canada
00817365020304Fusion 2K XL 42x80x8
00817365021669Fusion 2K XL 42 x 84 x 8
00817365021652Fusion 2K XL 48x84x8
00817365021638Fusion 2K XL 42x80x8
00817365022246Fusion APT Outer Cover 35x80x6
00817365022239Fusion 2K Outer Cover 35x84x6
00817365022222Fusion 2K Outer Cover 35x80x6
00817365022185Fusion 2K Cover 39x84x6
00817365022178Fusion 2K Cover 39x80x6

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.