SPY-Q™ or SPY-QCM™

GUDID 00858701006018

Novadaq Technologies Inc

Angiographic x-ray system application software

• Primary Device ID: 00858701006018
• NIH Device Record Key: e2a1bcc9-5c17-4ee0-bf24-3db73c68fd5f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SPY-Q™ or SPY-QCM™
• Version Model Number: SQ3500
• Company DUNS: 243730939
• Company Name: Novadaq Technologies Inc
• Device Count: 1
• 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: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• 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	00858701006018 [Primary]

FDA Product Code

• LLZ: System, Image Processing, Radiological

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-09-10
• 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
• 20858701006265 - SPY PAQ®: 2020-11-06