C5012A

GUDID 10845854030646

ACROMIOPLASTY ELECTRODE (ELECTRODE ONLY), QTY 5

Conmed Corporation

Endoscopic electrosurgical electrode, monopolar, single-use

• Primary Device ID: 10845854030646
• NIH Device Record Key: e50afd29-b883-4aa2-8ce0-d266ff1f5c17
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: C5012A
• Catalog Number: C5012A
• Company DUNS: 071595540
• Company Name: Conmed Corporation
• Device Count: 5
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00845854030649 [Unit of Use]
GS1	10845854030646 [Package]; Contains: 20845854030643; Package: BOX [5 Units]; In Commercial Distribution
GS1	20845854030643 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K823424

FDA Product Code

• HAW: Neurological stereotaxic Instrument

Sterilization

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

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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