Salute RDX FC-MOX0032

GUDID 00817365021539

Salute RDX Pump

MOXI ENTERPRISES, LLC

Low-air-loss bed
Primary Device ID00817365021539
NIH Device Record Key1c0ba57a-848b-456c-88f2-2c39d93a581d
Commercial Distribution StatusIn Commercial Distribution
Brand NameSalute RDX
Version Model NumberFC-MOX0032
Catalog NumberFC-MOX0032
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

Customer Support Contacts

Phone3147715222
Emailinfo@moxiusa.com
Phone3147715222
Emailinfo@moxiusa.com
Phone3147715222
Emailinfo@moxiusa.com
Phone3147715222
Emailinfo@moxiusa.com
Phone3147715222
Emailinfo@moxiusa.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100817365021539 [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 Date2022-05-26
Device Publish Date2022-05-18

On-Brand Devices [Salute RDX]

00817365021539Salute RDX Pump
00817365021362Salute RDX Mattress

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