T1030B

GUDID 30845854031692

10MM, 30 DEGREE EXTENDED LENGTH AUTOCLAVABLE EYECUP LAPAROSCOPE

Conmed Corporation

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• Primary Device ID: 30845854031692
• NIH Device Record Key: 52fd0a8b-90dd-4fad-9f87-8bd42641347a
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: T1030B
• Catalog Number: T1030B
• 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: 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(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
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com

Device Dimensions

• Device Size Text, specify: 0
• Angle: 30 degree
• Device Size Text, specify: 0
• Angle: 30 degree
• Device Size Text, specify: 0
• Angle: 30 degree
• Device Size Text, specify: 0
• Angle: 30 degree
• Device Size Text, specify: 0
• Angle: 30 degree
• Device Size Text, specify: 0
• Angle: 30 degree
• Device Size Text, specify: 0
• Angle: 30 degree
• Device Size Text, specify: 0
• Angle: 30 degree
• Device Size Text, specify: 0
• Angle: 30 degree
• Device Size Text, specify: 0
• Angle: 30 degree
• Device Size Text, specify: 0
• Angle: 30 degree
• Device Size Text, specify: 0
• Angle: 30 degree
• Device Size Text, specify: 0
• Angle: 30 degree
• Device Size Text, specify: 0
• Angle: 30 degree
• Device Size Text, specify: 0
• Angle: 30 degree
• Device Size Text, specify: 0
• Angle: 30 degree
• Device Size Text, specify: 0
• Angle: 30 degree
• Device Size Text, specify: 0
• Angle: 30 degree
• Device Size Text, specify: 0
• Angle: 30 degree
• Device Size Text, specify: 0
• Angle: 30 degree

Device Identifiers

Device Issuing Agency	Device ID
GS1	20845854031695 [Primary]
GS1	30845854031692 [Direct Marking]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K050163

FDA Product Code

• GCJ: Laparoscope, general & plastic surgery

Sterilization

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

[30845854031692]

Moist Heat or Steam Sterilization

[30845854031692]

Moist Heat or Steam Sterilization

[30845854031692]

Moist Heat or Steam Sterilization

[30845854031692]

Moist Heat or Steam Sterilization

[30845854031692]

Moist Heat or Steam Sterilization

[30845854031692]

Moist Heat or Steam Sterilization

[30845854031692]

Moist Heat or Steam Sterilization

[30845854031692]

Moist Heat or Steam Sterilization

[30845854031692]

Moist Heat or Steam Sterilization

[30845854031692]

Moist Heat or Steam Sterilization

[30845854031692]

Moist Heat or Steam Sterilization

[30845854031692]

Moist Heat or Steam Sterilization

[30845854031692]

Moist Heat or Steam Sterilization

[30845854031692]

Moist Heat or Steam Sterilization

[30845854031692]

Moist Heat or Steam Sterilization

[30845854031692]

Moist Heat or Steam Sterilization

[30845854031692]

Moist Heat or Steam Sterilization

[30845854031692]

Moist Heat or Steam Sterilization

[30845854031692]

Moist Heat or Steam Sterilization

[30845854031692]

Moist Heat or Steam Sterilization

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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• 30845854027862 - GENESYS PressFT, Hi-Fi: 2024-04-25 GENESYS PressFT 2.1 w/One #2 (5 metric) Hi-Fi Suture, HIP (1 White/Black)
• 30845854027893 - GENESYS PressFT, Hi-Fi: 2024-04-25 GENESYS PressFT 2.6 w/One #2 (5 metric) Hi-Fi Suture, HIP (1 White/Black)
• 30845854034600 - GENESYS CrossFT, Hi-Fi: 2024-04-25 GENESYS CrossFT 5.5 mm Suture Anchor, w/3 Hi-Fi #2 (5 metric) Sutures w/Needles
• 30845854034617 - GENESYS CrossFT, Hi-Fi: 2024-04-25 GENESYS CrossFT 6.5 mm Suture Anchor, w/2 Hi-Fi #2 (5 metric) Sutures w/Needles
• 30653405988643 - Argo Knotless GENESYS: 2024-04-22 5.5mm Argo Knotless® GENESYSTM Anchor