Simon Nitinol Filter™ 2120F

GUDID 00801741040900

Simon Nitinol Filter™ Femoral Delivery Set

Bard Peripheral Vascular, Inc.

Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent
Primary Device ID00801741040900
NIH Device Record Keyf471d7e7-e004-4154-9860-362d7926e295
Commercial Distribution StatusIn Commercial Distribution
Brand NameSimon Nitinol Filter™
Version Model Number2120F
Catalog Number2120F
Company DUNS135057938
Company NameBard Peripheral Vascular, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Safe
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

Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.com
Phone+1(800)321-4254
Emailmedical.services@crbard.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 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
GS100801741040900 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DTKFILTER, INTRAVASCULAR, CARDIOVASCULAR

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2015-10-02

On-Brand Devices [Simon Nitinol Filter™]

00801741109218Simon Nitinol Filter™ , Vena Cava Filter, Anticubital Introducer Set
00801741109195Simon Nitinol Filter™ , Vena Cava Filter, Jugular Introducer Set
00801741109188Simon Nitinol Filter™ , Vena Cava Filter, Femoral Introducer Set
00801741040924Simon Nitinol Filter™ Antecubital Filter Set
00801741040917Simon Nitinol Filter™ Jugular/Subclavian Delivery Set
00801741040900Simon Nitinol Filter™ Femoral Delivery Set

Trademark Results [Simon Nitinol Filter]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SIMON NITINOL FILTER
SIMON NITINOL FILTER
73747821 1556677 Live/Registered
NITINOL MEDICAL TECHNOLOGIES, INC.
1988-08-23

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