HD4301RFB

GUDID 20845854044206

RFB, 4MM, 30 DEGREE HD QUICKLATCH AUTOCLAVABLE CARTRIDGE SCOPE

Conmed Corporation

Rigid arthroscope, reusable

• Primary Device ID: 20845854044206
• NIH Device Record Key: 425901d0-1b84-46de-9977-db9aa6cccd8b
• Commercial Distribution Discontinuation: 2022-06-06
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: HD4301RFB
• Catalog Number: HD4301RFB
• 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: false
• Serial Number: true
• 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
• 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 Dimensions

• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree
• Outer Diameter: 4 Millimeter
• Angle: 30 degree

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY

Device Identifiers

Device Issuing Agency	Device ID
GS1	10845854044209 [Primary]
GS1	20845854044206 [Direct Marking]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K962075

FDA Product Code

• HRX: ARTHROSCOPE

Sterilization

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

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

[20845854044206]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2022-06-07
• Device Publish Date: 2016-10-14

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