Headway MC272156S

GUDID 00811425021385

Microcatheter

MICROVENTION INC.

Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter Vascular microcatheter
Primary Device ID00811425021385
NIH Device Record Key0d32f72c-7293-48ce-9a15-ba53217bc823
Commercial Distribution StatusIn Commercial Distribution
Brand NameHeadway
Version Model NumberMC272156S
Catalog NumberMC272156S
Company DUNS003263105
Company NameMICROVENTION INC.
Device Count1
DM Exempttrue
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 Latextrue
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
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 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
GS100811425021385 [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 Date2016-09-24

On-Brand Devices [Headway]

00811425021385Microcatheter
00811425020449Microcatheter
00810170016165Microcatheter
00810170014857Microcatheter
00812636020945Microcatheter
04987350609199Microcatheter

Trademark Results [Headway]

Mark Image

Registration | Serial
Company
Trademark
Application Date
HEADWAY
HEADWAY
98063420 not registered Live/Pending
Dycom Industries, Inc.
2023-06-28
HEADWAY
HEADWAY
97809660 not registered Live/Pending
GUANGRAO GEE-STAR TIRE CO., LTD.
2023-02-24
HEADWAY
HEADWAY
97574738 not registered Live/Pending
Protonex LLC
2022-09-01
HEADWAY
HEADWAY
97111170 not registered Live/Pending
Dycom Industries, Inc.
2021-11-05
HEADWAY
HEADWAY
90656812 not registered Live/Pending
GTHW APP LIMITED
2021-04-20
HEADWAY
HEADWAY
90652554 not registered Live/Pending
Shipped Accessories LLC
2021-04-17
HEADWAY
HEADWAY
88155195 5836282 Live/Registered
Therapymatch, Inc.
2018-10-15
HEADWAY
HEADWAY
87452083 5323914 Live/Registered
Already, LLC
2017-05-16
HEADWAY
HEADWAY
86386332 not registered Dead/Abandoned
Headway App, LLC
2014-09-05
HEADWAY
HEADWAY
85513415 4321839 Live/Registered
Headway Marketing, LLC
2012-01-10
HEADWAY
HEADWAY
79364152 not registered Live/Pending
Angelini Pharma S.p.A.
2022-12-20
HEADWAY
HEADWAY
79060074 3654997 Live/Registered
Zhejiang Headway Communication Equipment Co., Ltd.
2008-08-09

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