LUNA PAQ®

GUDID 10858701006244

Novadaq Technologies Inc

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