LUNA PAQ®

GUDID 10858701006244

Novadaq Technologies Inc

General surgical procedure kit, medicated General surgical procedure kit, medicated General surgical procedure kit, medicated General surgical procedure kit, medicated General surgical procedure kit, medicated General surgical procedure kit, medicated General surgical procedure kit, medicated

• Primary Device ID: 10858701006244
• NIH Device Record Key: 9da9af73-afbc-4576-8c9b-d982f78a64a5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LUNA PAQ®
• Version Model Number: LU3001
• Company DUNS: 243730939
• Company Name: Novadaq Technologies 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: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10858701006244 [Primary]
GS1	20858701006241 [Package]; Package: box [6 Units]; In Commercial Distribution

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-11-06
• Device Publish Date: 2016-09-23

Devices Manufactured by Novadaq Technologies Inc

• 20858701006326 - SPY-PHI System: 2024-02-29 SPY-PHI drape
• 10858701006220 - PINPOINT PAQ®: 2023-10-30
• 20858701006258 - SPY®: 2023-10-30
• 10858701006299 - NOVADRAPE®: 2023-10-30 sterile drape
• 10858701006176 - PINPOINT PAQ®: 2020-11-06
• 10858701006237 - PINPOINT PAQ®: 2020-11-06
• 10858701006244 - LUNA PAQ®: 2020-11-06
• 10858701006244 - LUNA PAQ®: 2020-11-06
• 20858701006265 - SPY PAQ®: 2020-11-06