Millennium 5

GUDID 00815871021401

Avante

Orthopaedic stretcher
Primary Device ID00815871021401
NIH Device Record Key1e8c84b4-1705-49cd-bd6a-d5cab3d5edbb
Commercial Distribution StatusIn Commercial Distribution
Brand NameMillennium 5
Version Model Number7JE200EXT
Company DUNS178440426
Company NameAvante
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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone502-244-4444
Emaildevicehelp@dremed.com
Phone502-244-4444
Emaildevicehelp@dremed.com
Phone502-244-4444
Emaildevicehelp@dremed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100815871021401 [Primary]

FDA Product Code

FPOStretcher, Wheeled

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-06-19
Device Publish Date2016-09-23

On-Brand Devices [Millennium 5]

008158710214017JE200EXT
008158710205277JE200

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