HELIXAR 60-8432-001

GUDID 30653405001960

HELIXAR CART

Conmed Corporation

Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system
Primary Device ID30653405001960
NIH Device Record Keyd90fdf18-f707-4dbe-ab20-632ab5b3b801
Commercial Distribution StatusIn Commercial Distribution
Brand NameHELIXAR
Version Model Number60-8432-001
Catalog Number60-8432-001
Company DUNS071595540
Company NameConmed Corporation
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 Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS130653405001960 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIElectrosurgical, cutting & coagulation & accessories

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number2
Public Version Date2018-07-06
Device Publish Date2018-03-20

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30653405001960HELIXAR CART
20653405001994HELIXAR STACKING ADAPTER FOR SYSTEM 5000 ELECTROSURGICAL UNIT STACKING ADAPTER
20653405001987SMOKE KIT, HELIXAR AER DEFENSE DOOR ASSEMBLY
20653405001963HELIXAR CART
30653405000758HELIXAR:GENERATOR, CART, MONO F/S, BI F/S
10653405001966HELIXAR CART
10653405005537HELIXAR 100 - 240 VAC 50/60 HZ ELECTROSURGICAL UNIT WITH ARGON BEAM COAGULATOR

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