Q37264

GUDID 10653405001911

KIT PACK-LARGE,TROCAR

Conmed Corporation

Laparoscopic surgical procedure kit, non-medicated, single-use

• Primary Device ID: 10653405001911
• NIH Device Record Key: f10a0238-de6f-406c-b0af-dbde961cbd6c
• Commercial Distribution Discontinuation: 2020-12-08
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: Q37264
• Catalog Number: Q37264
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10653405001911 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K924761

FDA Product Code

• GCJ: Laparoscope, general & plastic surgery

Sterilization

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

[10653405001911]

Ethylene Oxide

[10653405001911]

Ethylene Oxide

[10653405001911]

Ethylene Oxide

[10653405001911]

Ethylene Oxide

[10653405001911]

Ethylene Oxide

[10653405001911]

Ethylene Oxide

[10653405001911]

Ethylene Oxide

[10653405001911]

Ethylene Oxide

[10653405001911]

Ethylene Oxide

[10653405001911]

Ethylene Oxide

[10653405001911]

Ethylene Oxide

[10653405001911]

Ethylene Oxide

[10653405001911]

Ethylene Oxide

[10653405001911]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-12-08
• Device Publish Date: 2016-09-24

Devices Manufactured by Conmed Corporation

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• 10653405063797 - CONMED: 2026-04-01 CONMED ECG LEADWIRES, 5 LEADS, 28"
• 00845854035590 - CONCEPT: 2026-04-01 CONCEPT ABLATOR ELECTRODE, 90 DEGREE (ELECTRODE ONLY), QTY 5
• 10845854041116 - POWERPRO: 2026-04-01 POWERPRO UNIVERSAL CONTROLLER 115V
• 10845854041291 - CONMED: 2026-04-01 XENON REPLACEMENT BULB, 300 WATT
• 00653405014952 - POOLE: 2026-04-01 POOLE Suction Instrument with Removable Sheath and 10' (3.0 m) Clear Plastic Tubing
• 20653405017759 - CONMED: 2026-04-01 CABLE, SHIELD, 3 LEADS, CONN 3
• 20653405017766 - CONMED: 2026-04-01 ECG MONITOR CABLE