SideFire® Directional Laser Probe NBP-201-01

GUDID 00816589020571

3.3mm Directional Laser Probe

MONTERIS MEDICAL INC

MRI-guided laser interstitial thermal therapy system beam guide

• Primary Device ID: 00816589020571
• NIH Device Record Key: 333f0fb8-96c3-4c6f-9c02-9b8e983b994c
• Commercial Distribution Discontinuation: 2017-10-25
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: SideFire® Directional Laser Probe
• Version Model Number: 20368-2
• Catalog Number: NBP-201-01
• Company DUNS: 021415875
• Company Name: MONTERIS MEDICAL INC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• 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(866)799-7655
• Email: info@monteris.com
• Phone: +1(866)799-7655
• Email: info@monteris.com
• Phone: +1(866)799-7655
• Email: info@monteris.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 Identifiers

Device Issuing Agency	Device ID
GS1	00816589020571 [Primary]

FDA Product Code

• GEX: Powered Laser Surgical 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: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-03-10

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