WEB W5-4.5-2

GUDID 00842429110799

WEB 17 SL 4.5x2

MICROVENTION INC.

Neurovascular embolization coil Neurovascular embolization coil Neurovascular embolization coil Neurovascular embolization coil Neurovascular embolization coil Neurovascular embolization coil Neurovascular embolization coil Neurovascular embolization coil Neurovascular embolization coil Neurovascular embolization coil Neurovascular embolization coil Neurovascular embolization coil Neurovascular embolization coil Neurovascular embolization coil
Primary Device ID00842429110799
NIH Device Record Key033e6da3-a960-4640-a733-625e3d2889f2
Commercial Distribution StatusIn Commercial Distribution
Brand NameWEB
Version Model NumberW5-4.5-2-MVI-3
Catalog NumberW5-4.5-2
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 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

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 Identifiers

Device Issuing AgencyDevice ID
GS100842429110799 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OPRIntrasaccular Flow Disruption Device

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-06-08
Device Publish Date2021-05-31

On-Brand Devices [WEB]

00842429110966WEB 17 SLS 7
00842429110959WEB 17 SL 7x6
00842429110942WEB 17 SL 7x5
00842429110935WEB 17 SL 7x4
00842429110928WEB 17 SL 7x3
00842429110911WEB 17 SLS 6
00842429110904WEB 17 SL 6x5
00842429110898WEB 17 SL 6x4
00842429110881WEB 17 SL 6x3
00842429110874WEB 17 SLS 5
00842429110867WEB 17 SL 5x4
00842429110850WEB 17 SL 5x3
00842429110843WEB 17 SL 5x2
00842429110836WEB 17 SLS 4
00842429110829WEB 17 SL 4x3
00842429110812WEB 17 SL 4x2
00842429110805WEB 17 SL 4.5x3
00842429110799WEB 17 SL 4.5x2

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