ILLUMISITE

GUDID 20884521807980

Patient Sensor Patches

Covidien LP

Hypoallergenic skin adhesive tape Hypoallergenic skin adhesive tape Hypoallergenic skin adhesive tape Hypoallergenic skin adhesive tape Hypoallergenic skin adhesive tape Hypoallergenic skin adhesive tape Hypoallergenic skin adhesive tape Hypoallergenic skin adhesive tape Hypoallergenic skin adhesive tape Hypoallergenic skin adhesive tape Hypoallergenic skin adhesive tape Hypoallergenic skin adhesive tape Hypoallergenic skin adhesive tape Hypoallergenic skin adhesive tape Hypoallergenic skin adhesive tape Hypoallergenic skin adhesive tape

• Primary Device ID: 20884521807980
• NIH Device Record Key: 1cc05510-812a-43b4-9bce-671785c98474
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ILLUMISITE
• Version Model Number: ILS-1000-SP
• Company DUNS: 058614483
• Company Name: Covidien LP
• Device Count: 60
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10884521807983 [Primary]
GS1	20884521807980 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K191394

FDA Product Code

• JAK: System, x-ray, tomography, computed

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: 2021-11-02
• Device Publish Date: 2020-11-04

On-Brand Devices [ILLUMISITE]

• 10884521779990: Planning Software V1.0
• 10884521779983: Procedure Software V1.0
• 10884521723993: Bronchoscope Adapter for se with Fujinon bronchoscopes
• 10884521723986: Bronchoscope Adapter for use with Pentax bronchoscopes
• 10884521723979: Bronchocope Adapter for use with Olyumpus 190 bronchoscope
• 10884521723962: Bronchoscope Adapter for use with Olympus bronchoscopes
• 10884521723955: Patient Sensor Patch
• 10884521723801: Bronchoscope Adapter for use with Fujinon bronchoscopes
• 10884521723795: Bronchoscope Adapter for use with Pentax bronchoscopes
• 10884521723788: Bronchoscope Adapter for use with Olympus 190 bronchoscopes
• 10884521723771: Bronchoscope Adapter for use with Olympus bronchoscopes
• 10884521723634: Console
• 10884521723832: Endobronchial Procedure Kit 45 Catheter
• 10884521723825: Endobronchial Procedure Kit 90 Catheter
• 10884521723818: Endobronchial Procedure Kit 180 Catheter
• 10884521812383: ILS-1000-CS ILLUMISITE CONSOLE EU
• 20884521807980: Patient Sensor Patches
• 10884521812413: Endobronchial Procedure Kit 45 Catheter
• 20884521842424: Patient Sensor Patches
• 10884521837096: Console