Compact Plus

GUDID 00815871020268

Avante

Foetal cardiac monitor
Primary Device ID00815871020268
NIH Device Record Key6f0f0c49-86e9-4dda-b68c-28db022c6249
Commercial Distribution StatusIn Commercial Distribution
Brand NameCompact Plus
Version Model Number60131EXP2
Company DUNS178440426
Company NameAvante
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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

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

Device Identifiers

Device Issuing AgencyDevice ID
GS100815871020268 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HGMSystem, Monitoring, Perinatal

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-03-02
Device Publish Date2016-09-23

On-Brand Devices [Compact Plus]

0081587102028260131EXPI
0081587102027560131I
0081587102026860131EXP2
0081587102025160131B
0081587102024460131EXP
0081587102023760131

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