PowerWire Radiofrequency GuideWire Kit

GUDID 00685447001041

PowerWire RF GuideWire; RFP-100A Connector Cable

Baylis Médicale Cie Inc

Endoscopic electrosurgical electrode, monopolar, single-use
Primary Device ID00685447001041
NIH Device Record Key2f54b45f-d1f4-45a4-ba37-a7a3af843c54
Commercial Distribution StatusIn Commercial Distribution
Brand NamePowerWire Radiofrequency GuideWire Kit
Version Model NumberEWK35-250-10-6S
Company DUNS249225954
Company NameBaylis Médicale Cie Inc
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com
Phone5144889801
Emailinfo@baylismedical.com

Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS100685447001041 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

PDUCatheter For Crossing Total Occlusions

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-13

On-Brand Devices [PowerWire Radiofrequency GuideWire Kit]

00685447002161PowerWire RF GuideWire; RFP-100A Connector Cable
00685447002154PowerWire RF GuideWire; RFP-100A Connector Cable
00685447002147PowerWire RF GuideWire; RFP-100A Connector Cable
00685447001089PowerWire RF GuideWire; RFP-100A Connector Cable
00685447001072PowerWire RF GuideWire; RFP-100A Connector Cable
00685447001065PowerWire RF GuideWire; RFP-100A Connector Cable
00685447001058PowerWire RF GuideWire; RFP-100A Connector Cable
00685447001041PowerWire RF GuideWire; RFP-100A Connector Cable
00685447001034PowerWire RF GuideWire; RFP-100A Connector Cable

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