SCOPEPORT™ 080200

GUDID 00850200006872

SCOPEPORT™ KIT

LSI Solutions, Inc.

Pleuroscopic/mediastinoscopic access cannula, single-use Pleuroscopic/mediastinoscopic access cannula, single-use Pleuroscopic/mediastinoscopic access cannula, single-use Pleuroscopic/mediastinoscopic access cannula, single-use Pleuroscopic/mediastinoscopic access cannula, single-use Pleuroscopic/mediastinoscopic access cannula, single-use Pleuroscopic/mediastinoscopic access cannula, single-use Pleuroscopic/mediastinoscopic access cannula, single-use

• Primary Device ID: 00850200006872
• NIH Device Record Key: 92075ec6-bb3e-4a0b-a882-79fb227ed914
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SCOPEPORT™
• Version Model Number: 080200
• Catalog Number: 080200
• Company DUNS: 603420183
• Company Name: LSI Solutions, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• 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(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com

Device Dimensions

• Length: 8 Inch
• Lumen/Inner Diameter: 5 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Lumen/Inner Diameter: 5 Millimeter
• Lumen/Inner Diameter: 5 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850200006872 [Primary]

FDA Product Code

• GEA: CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY

Sterilization

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

[00850200006872]

Moist Heat or Steam Sterilization

[00850200006872]

Moist Heat or Steam Sterilization

[00850200006872]

Moist Heat or Steam Sterilization

[00850200006872]

Moist Heat or Steam Sterilization

[00850200006872]

Moist Heat or Steam Sterilization

[00850200006872]

Moist Heat or Steam Sterilization

[00850200006872]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-03-30
• Device Publish Date: 2020-03-13

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