Savoy QA3

GUDID 00815871020589

Avante

Orthopaedic stretcher
Primary Device ID00815871020589
NIH Device Record Key0440bc75-b001-489c-a5c9-00b6ba4b4eca
Commercial Distribution StatusIn Commercial Distribution
Brand NameSavoy QA3
Version Model Number7QA3MES
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
GS100815871020589 [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 [Savoy QA3]

008158710205967QA3MD
008158710205897QA3MES
008158710205727QA3MXP
008158710205657QA3M

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