FloWire Floppy Doppler Guide Wire JTIP

GUDID 00184360000129

VOLCANO CORPORATION

Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler Blood flowmeter catheter, Doppler
Primary Device ID00184360000129
NIH Device Record Keyc1b3df79-e31f-46d4-aaa9-4254ec3da923
Commercial Distribution StatusIn Commercial Distribution
Brand NameFloWire Floppy Doppler Guide Wire JTIP
Version Model Number1400J
Company DUNS135179237
Company NameVOLCANO CORPORATION
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 Usetrue
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com
Phone(800) 228-4728
EmailIGTD.CustomerInquiry@philips.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100184360000129 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DQXWire, Guide, Catheter

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 Date2016-08-24

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