7453

GUDID 20845854018030

LIGHT GUIDE FITTING FOR STORZ, OLYMPUS, AND LINVATEC SCOPES

Conmed Corporation

Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source unit, line-powered Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor Endoscopic light source adaptor

• Primary Device ID: 20845854018030
• NIH Device Record Key: 0872c10d-adf3-4b82-bc30-b7fe02c0ccbe
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 7453
• Catalog Number: 7453
• Company DUNS: 071595540
• Company Name: Conmed Corporation
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• 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(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10845854018033 [Primary]
GS1	20845854018030 [Direct Marking]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K850749

FDA Product Code

• KQM: CAMERA, SURGICAL AND ACCESSORIES

Sterilization

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

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

[20845854018030]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2022-06-30
• Device Publish Date: 2020-09-24

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• 30653405988698 - Argo Knotless GENESYS: 2024-04-22 4.75mm Argo Knotless® GENESYSTM Anchor, HI-FI Tape, White/Black
• 30653405988735 - Argo Knotless GENESYS: 2024-04-22 5.5 mm Argo KnotlessTM GENESYSTM Disposable Tap
• 30653405988742 - Argo Knotless GENESYS: 2024-04-22 4.75 mm Argo KnotlessTM GENESYSTM Disposable Tap