Barrx 90-9100

GUDID 10884521189362

90 RFA Focal Catheter,80 Applications

Covidien LP

Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Endoscopic electrosurgical handpiece/electrode, bipolar, single-use Gastrointestinal radio-frequency ablation system catheter Gastrointestinal radio-frequency ablation system catheter Gastrointestinal radio-frequency ablation system catheter Gastrointestinal radio-frequency ablation system catheter Gastrointestinal radio-frequency ablation system catheter Gastrointestinal radio-frequency ablation system catheter Gastrointestinal radio-frequency ablation system catheter Gastrointestinal radio-frequency ablation system catheter Gastrointestinal radio-frequency ablation system catheter Gastrointestinal radio-frequency ablation system catheter Gastrointestinal radio-frequency ablation system catheter Gastrointestinal radio-frequency ablation system catheter Gastrointestinal radio-frequency ablation system catheter Gastrointestinal radio-frequency ablation system catheter Gastrointestinal radio-frequency ablation system catheter Gastrointestinal radio-frequency ablation system catheter Gastrointestinal radio-frequency ablation system catheter
Primary Device ID10884521189362
NIH Device Record Key343c062f-f352-48e3-9222-1de3ff1e7279
Commercial Distribution StatusIn Commercial Distribution
Brand NameBarrx
Version Model Number90-9100
Catalog Number90-9100
Company DUNS058614483
Company NameCovidien LP
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

Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com

Device Dimensions

Length13 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter
Width13 Millimeter
Length20 Millimeter

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *;

Device Identifiers

Device Issuing AgencyDevice ID
GS110884521189362 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-04-23
Device Publish Date2016-09-24

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Trademark Results [Barrx]

Mark Image

Registration | Serial
Company
Trademark
Application Date
BARRX
BARRX
85560393 4221763 Live/Registered
COVIDIEN LP
2012-03-05

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