9735BA

GUDID 20845854026073

MENISCECTOMY ELECTRODE BASIC KIT; STANDARD DESIGN

Conmed Corporation

Arthroscopic surgical procedure kit, non-medicated, single-use

• Primary Device ID: 20845854026073
• NIH Device Record Key: 4d66727e-5265-4dfc-b49e-281c7aba8680
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 9735BA
• Catalog Number: 9735BA
• Company DUNS: 071595540
• Company Name: Conmed Corporation
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	20845854026073 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K823424

FDA Product Code

• HAW: Neurological stereotaxic Instrument

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: true

[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 Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-24

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