BEAMER S-BEAM-3

GUDID 20653405986468

BEAMER ARGON SIDEFIRE PROBE, SIDEFIRE PROBE FOR FLEXIBLE ENDOSCOPY

Conmed Corporation

Argon-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use

• Primary Device ID: 20653405986468
• NIH Device Record Key: 593deb22-040d-4380-b8ef-efd9f737de5b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BEAMER
• Version Model Number: S-BEAM-3
• Catalog Number: S-BEAM-3
• Company DUNS: 071595540
• Company Name: Conmed Corporation
• Device Count: 10
• DM Exempt: true
• 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
• 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 Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY

Device Identifiers

Device Issuing Agency	Device ID
GS1	00653405986464 [Unit of Use]
GS1	10653405986461 [Primary]
GS1	20653405986468 [Package]; Contains: 10653405986461; Package: BOX [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K081644

FDA Product Code

• GEI: Electrosurgical, cutting & coagulation & accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-04-23
• Device Publish Date: 2019-04-15

On-Brand Devices [BEAMER]

• 10653405064206: BEAMER ARGON SNARE PROBE
• 10653405064190: BEAMER ARGON SNARE PROBE
• 10653405064183: BEAMER ARGON SNARE PROBE
• 10653405064176: BEAMER ARGON SNARE PROBE
• 10653405064169: BEAMER ARGON SNARE PROBE
• 20653405986468: BEAMER ARGON SIDEFIRE PROBE, SIDEFIRE PROBE FOR FLEXIBLE ENDOSCOPY