Q50 Plus Q50-100P

GUDID 00853892004010

Q50 Plus Stent Graft Balloon Catheter, 100cm

QXMEDICAL

Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided Intravascular occluding balloon catheter, image-guided
Primary Device ID00853892004010
NIH Device Record Key7546fa74-54e3-48a7-9546-c3dbc8cadc69
Commercial Distribution StatusIn Commercial Distribution
Brand NameQ50 Plus
Version Model NumberQ50-100P
Catalog NumberQ50-100P
Company DUNS022672652
Company NameQXMEDICAL
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 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

Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com
Phone651-842-2050
Emailadmin@qxmedical.com

Device Dimensions

Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter
Length100 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100853892004010 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DQYCatheter, Percutaneous

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-03-21
Device Publish Date2016-06-08

On-Brand Devices [Q50 Plus]

00853892004010Q50 Plus Stent Graft Balloon Catheter, 100cm
00853892004003Q50 Plus Stent Graft Balloon Catheter, 65cm

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