UHD4700CM

GUDID 10845854083420

4.0mm, 70° UHD Quicklatch C-Mount Arthroscope, 157 mm WL

Conmed Corporation

Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable Rigid arthroscope, reusable

• Primary Device ID: 10845854083420
• NIH Device Record Key: 3667b5de-d255-4993-a3f7-4074c2331723
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: UHD4700CM
• Catalog Number: UHD4700CM
• 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: 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(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 Dimensions

• Length: 4 Millimeter
• Length: 4 Millimeter
• Length: 4 Millimeter
• Length: 4 Millimeter
• Length: 4 Millimeter
• Length: 4 Millimeter
• Length: 4 Millimeter
• Length: 4 Millimeter
• Length: 4 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	10845854083420 [Direct Marking]
GS1	30845854083424 [Primary]

FDA Product Code

• HRX: Arthroscope

Sterilization

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

[10845854083420]

Moist Heat or Steam Sterilization

[10845854083420]

Moist Heat or Steam Sterilization

[10845854083420]

Moist Heat or Steam Sterilization

[10845854083420]

Moist Heat or Steam Sterilization

[10845854083420]

Moist Heat or Steam Sterilization

[10845854083420]

Moist Heat or Steam Sterilization

[10845854083420]

Moist Heat or Steam Sterilization

[10845854083420]

Moist Heat or Steam Sterilization

[10845854083420]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-08-30
• Device Publish Date: 2021-08-21

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• 10845854027868 - GENESYS PRESSFT: 2024-04-18 GENESYS PRESS FT 2.1 W/ONE # 2 (5 METRIC) HI-FI SUTURE, HIP
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