Trumpf TRUMPFKIT02

GUDID 30845854081000

Trumpf Medical Kit

Conmed Corporation

Surgical plume evacuation system

• Primary Device ID: 30845854081000
• NIH Device Record Key: c207f608-3775-4f50-a064-3cfe76e0bf90
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Trumpf
• Version Model Number: TRUMPFKIT02
• Catalog Number: TRUMPFKIT02
• 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: true
• 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
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	30845854081000 [Primary]

FDA Product Code

• FYD: APPARATUS, EXHAUST, SURGICAL

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-08-12
• Device Publish Date: 2020-11-19

Devices Manufactured by Conmed Corporation

• 00810021867373 - CoLink®: 2025-07-11 CoLink® Afx, Locking Screw, 2.7X14.0MM, 2-Pack
• 00810021867380 - CoLink®: 2025-07-11 CoLink® Afx, Locking Screw, 2.7X16.0MM, 2-Pack
• 00810021867403 - CoLink®: 2025-07-11 CoLink® Afx, Locking Screw, 3.5X12.0MM, 2-Pack
• 00810021867410 - CoLink®: 2025-07-11 CoLink® Afx, Locking Screw, 3.5X14.0MM, 2-Pack
• 00810021867427 - CoLink®: 2025-07-11 CoLink® Afx, LOW-PRO CORTICAL SCREW, 3.5X12.0MM, 2-Pack
• 00810021867434 - CoLink®: 2025-07-11 CoLink® Afx, LOW-PRO CORTICAL SCREW, 3.5X14.0MM, 2-Pack
• 08101755018714 - CoLink®: 2025-07-11 CoLink® Afx, Locking Screw, 3.5X10.0MM, 2-Pack
• 08101755018721 - CoLink®: 2025-07-11 CoLink® Afx, Locking Screw, 3.5X16.0MM, 2-Pack