9735BA

GUDID 20845854026073

MENISCECTOMY ELECTRODE BASIC KIT; STANDARD DESIGN

Conmed Corporation

Arthroscopic surgical procedure kit, non-medicated, single-use
Primary Device ID20845854026073
NIH Device Record Key4d66727e-5265-4dfc-b49e-281c7aba8680
Commercial Distribution StatusIn Commercial Distribution
Version Model Number9735BA
Catalog Number9735BA
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 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)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
GS120845854026073 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HAWNeurological stereotaxic Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[20845854026073]

Radiation Sterilization;Ethylene Oxide


[20845854026073]

Radiation Sterilization;Ethylene Oxide


[20845854026073]

Radiation Sterilization;Ethylene Oxide


[20845854026073]

Radiation Sterilization;Ethylene Oxide


[20845854026073]

Radiation Sterilization;Ethylene Oxide


[20845854026073]

Radiation Sterilization;Ethylene Oxide


[20845854026073]

Radiation Sterilization;Ethylene Oxide


[20845854026073]

Radiation Sterilization;Ethylene Oxide


[20845854026073]

Radiation Sterilization;Ethylene Oxide


[20845854026073]

Radiation Sterilization;Ethylene Oxide


[20845854026073]

Radiation Sterilization;Ethylene Oxide


[20845854026073]

Radiation Sterilization;Ethylene Oxide


[20845854026073]

Radiation Sterilization;Ethylene Oxide


[20845854026073]

Radiation Sterilization;Ethylene Oxide


[20845854026073]

Radiation Sterilization;Ethylene Oxide


[20845854026073]

Radiation Sterilization;Ethylene Oxide


[20845854026073]

Radiation Sterilization;Ethylene Oxide


[20845854026073]

Radiation Sterilization;Ethylene Oxide


[20845854026073]

Radiation Sterilization;Ethylene Oxide


[20845854026073]

Radiation Sterilization;Ethylene Oxide


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-24

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