FindrWIRZ FG-005

GUDID 10840143901751

FindrWIRZ Guide Wire System

ATRICURE, INC.

Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use
Primary Device ID10840143901751
NIH Device Record Keyf416b5ce-222e-4f26-acc3-91605f87a1f2
Commercial Distribution StatusIn Commercial Distribution
Brand NameFindrWIRZ
Version Model Number40-05
Catalog NumberFG-005
Company DUNS006133784
Company NameATRICURE, INC.
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

Phone650-354-1200
Emailinfo@sentreheart.com
Phone650-354-1200
Emailinfo@sentreheart.com
Phone650-354-1200
Emailinfo@sentreheart.com
Phone650-354-1200
Emailinfo@sentreheart.com
Phone650-354-1200
Emailinfo@sentreheart.com
Phone650-354-1200
Emailinfo@sentreheart.com
Phone650-354-1200
Emailinfo@sentreheart.com
Phone650-354-1200
Emailinfo@sentreheart.com
Phone650-354-1200
Emailinfo@sentreheart.com
Phone650-354-1200
Emailinfo@sentreheart.com
Phone650-354-1200
Emailinfo@sentreheart.com
Phone650-354-1200
Emailinfo@sentreheart.com
Phone650-354-1200
Emailinfo@sentreheart.com
Phone650-354-1200
Emailinfo@sentreheart.com
Phone650-354-1200
Emailinfo@sentreheart.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100818354017588 [Previous]
GS110840143901751 [Primary]
GS130840143901762 [Package]
Package: box [1 Units]
In Commercial Distribution
GS150840143901742 [Package]
Contains: 30840143901762
Package: case [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DQXWire, Guide, Catheter

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-01-19
Device Publish Date2021-01-11

On-Brand Devices [FindrWIRZ]

00818354017588FindrWIRZ Guidewire System
10840143901751FindrWIRZ Guide Wire System
30840143909522FindrWIRZ Guide Wire System

Trademark Results [FindrWIRZ]

Mark Image

Registration | Serial
Company
Trademark
Application Date
FINDRWIRZ
FINDRWIRZ
77540202 3719562 Live/Registered
SentreHEART, Inc.
2008-08-06

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