AVANOS* PMX-BAY-MRF

GUDID 00193493000289

Multi-Radiofrequency Module

Avanos Medical, Inc.

Electrosurgical cable adaptor Electrosurgical cable adaptor Electrosurgical cable adaptor Electrosurgical cable adaptor Electrosurgical cable adaptor Electrosurgical cable adaptor Electrosurgical cable adaptor Electrosurgical cable adaptor Electrosurgical cable adaptor Electrosurgical cable adaptor Electrosurgical cable adaptor Electrosurgical cable adaptor Electrosurgical cable adaptor Electrosurgical cable adaptor Electrosurgical cable adaptor Electrosurgical cable adaptor
Primary Device ID00193493000289
NIH Device Record Key03e1478f-37da-45b9-8ff4-1bb9bbbdd84b
Commercial Distribution StatusIn Commercial Distribution
Brand NameAVANOS*
Version Model NumberPMX-BAY-MRF
Catalog NumberPMX-BAY-MRF
Company DUNS079375431
Company NameAvanos Medical, Inc.
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 Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(844)428-2667
EmailPIQ@AVANOS.COM
Phone+1(844)428-2667
EmailPIQ@AVANOS.COM
Phone+1(844)428-2667
EmailPIQ@AVANOS.COM
Phone+1(844)428-2667
EmailPIQ@AVANOS.COM
Phone+1(844)428-2667
EmailPIQ@AVANOS.COM
Phone+1(844)428-2667
EmailPIQ@AVANOS.COM
Phone+1(844)428-2667
EmailPIQ@AVANOS.COM
Phone+1(844)428-2667
EmailPIQ@AVANOS.COM
Phone+1(844)428-2667
EmailPIQ@AVANOS.COM
Phone+1(844)428-2667
EmailPIQ@AVANOS.COM
Phone+1(844)428-2667
EmailPIQ@AVANOS.COM
Phone+1(844)428-2667
EmailPIQ@AVANOS.COM
Phone+1(844)428-2667
EmailPIQ@AVANOS.COM
Phone+1(844)428-2667
EmailPIQ@AVANOS.COM
Phone+1(844)428-2667
EmailPIQ@AVANOS.COM
Phone+1(844)428-2667
EmailPIQ@AVANOS.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS100193493000289 [Primary]

FDA Product Code

GXIProbe, radiofrequency lesion

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-03-25
Device Publish Date2022-03-17

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00193493000289Multi-Radiofrequency Module
40680651986786PMP-18-145

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