false MFX-TRAY

GUDID 30845854027732

INSTRUMENT TRAY, MICROFRACTURE AWL SET

Conmed Corporation

Instrument tray

• Primary Device ID: 30845854027732
• NIH Device Record Key: af68dc66-9010-41cd-ba2f-773a325219cb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: false
• Version Model Number: MFX-TRAY
• Catalog Number: MFX-TRAY
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• 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
• 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
• 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	20845854027735 [Primary]
GS1	30845854027732 [Direct Marking]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K080531

FDA Product Code

• KCT: Sterilization wrap containers, trays, cassettes & other accessories

Sterilization

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

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

[30845854027732]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2018-09-28
• Device Publish Date: 2016-09-24

Devices Manufactured by Conmed Corporation

• 30653405987585 - PlumeSafe® X5™: 2024-10-22 PlumeSafe® X5™ Smoke Evacuation Unit, 220V-240V 50/60 Hz
• 30653405987592 - PlumeSafe® X5™: 2024-10-22 PlumeSafe® X5™ Smoke Evacuation Unit with PlumeSafe® X5™ Smoke Evacuator Filter, 220V-240V 50/60 Hz
• 30653405987608 - PlumeSafe® X5™: 2024-10-22 PlumeSafe® X5™ Smoke Evacuation Unit, 220V-240V 50/60 Hz
• 30653405990141 - PlumeSafe® X5™: 2024-10-22 PlumeSafe® X5™ Smoke Evacuation Unit with PlumeSafe® X5™ Smoke Evacuator Filter, 220V-240V 50/60 Hz
• 20653405990120 - BioBrace: 2024-09-30 BioBrace® Reinforced Implant, 23 x 25 mm
• 20653405990137 - BioBrace: 2024-09-30 BioBrace® Reinforced Implant, 35 x 25 mm
• 20653405990144 - BioBrace: 2024-09-30 BioBrace® Reinforced Implant, 40 x 60 mm
• 20653405990151 - BioBrace: 2024-09-30 BioBrace® Reinforced Implant, Foot & Ankle, 40 x 60 mm