Stent FREDX3517

GUDID 00842429114308

FRED-X 27

MICROVENTION INC.

Bare-metal intracranial vascular stent
Primary Device ID00842429114308
NIH Device Record Keyddf2aa67-0d3f-4233-8a3c-73a9cf691089
Commercial Distribution StatusIn Commercial Distribution
Brand NameStent
Version Model NumberFREDX3517-PMA
Catalog NumberFREDX3517
Company DUNS003263105
Company NameMICROVENTION INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(714) 247-8000
Emailcustomerservice@microvention.com
Phone+1(714) 247-8000
Emailcustomerservice@microvention.com
Phone+1(714) 247-8000
Emailcustomerservice@microvention.com
Phone+1(714) 247-8000
Emailcustomerservice@microvention.com
Phone+1(714) 247-8000
Emailcustomerservice@microvention.com
Phone+1(714) 247-8000
Emailcustomerservice@microvention.com
Phone+1(714) 247-8000
Emailcustomerservice@microvention.com
Phone+1(714) 247-8000
Emailcustomerservice@microvention.com
Phone+1(714) 247-8000
Emailcustomerservice@microvention.com
Phone+1(714) 247-8000
Emailcustomerservice@microvention.com
Phone+1(714) 247-8000
Emailcustomerservice@microvention.com
Phone+1(714) 247-8000
Emailcustomerservice@microvention.com
Phone+1(714) 247-8000
Emailcustomerservice@microvention.com
Phone+1(714) 247-8000
Emailcustomerservice@microvention.com
Phone+1(714) 247-8000
Emailcustomerservice@microvention.com
Phone+1(714) 247-8000
Emailcustomerservice@microvention.com
Phone+1(714) 247-8000
Emailcustomerservice@microvention.com
Phone+1(714) 247-8000
Emailcustomerservice@microvention.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100842429114308 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OUTIntracranial aneurysm flow diverter

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2022-10-10
Device Publish Date2022-04-11

On-Brand Devices [Stent]

00842429114490FRED-X 27
00842429114483FRED-X 27
00842429114476FRED-X 27
00842429114469FRED-X 27
00842429114452FRED-X 27
00842429114445FRED-X 27
00842429114438FRED-X 27
00842429114421FRED-X 27
00842429114414FRED-X 27
00842429114407FRED-X 27
00842429114391FRED-X 27
00842429114384FRED-X 27
00842429114377FRED-X 27
00842429114360FRED-X 27
00842429114353FRED-X 27
00842429114346FRED-X 27
00842429114339FRED-X 27
00842429114322FRED-X 27
00842429114315FRED-X 27
00842429114308FRED-X 27
00842429114292FRED-X 27
00842429114285FRED-X 21
00842429114278FRED-X 21
00842429114261FRED-X 21
00842429114254FRED-X 21
00842429114247FRED-X 21
00842429114230FRED-X 21
00842429114223FRED-X 21
00842429114216FRED-X 21
00842429117903LVIS EVO
00842429117897LVIS EVO
00842429117880LVIS EVO
00842429117873LVIS EVO
00842429117866LVIS EVO
00842429117859LVIS EVO
00842429117842LVIS EVO
00842429117835LVIS EVO
00842429117828LVIS EVO
00842429117811LVIS EVO
00842429117804LVIS EVO
00842429117798LVIS EVO
00842429117781LVIS EVO
00842429117774LVIS EVO
00842429117767LVIS EVO
00842429117750LVIS EVO
00842429117743LVIS EVO

Trademark Results [Stent]

Mark Image

Registration | Serial
Company
Trademark
Application Date
STENT
STENT
79230782 not registered Dead/Abandoned
Air Bag Stopper Holdings Limited
2018-01-18

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.