PINPOINT PAQ®

GUDID 00858701006186

Novadaq Technologies Inc

Laparoscopic surgical procedure kit, non-medicated, single-use

• Primary Device ID: 00858701006186
• NIH Device Record Key: cd2c56f0-448d-4365-8de0-6384896adafc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PINPOINT PAQ®
• Version Model Number: PP9050
• 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: 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	00858701006186 [Primary]

FDA Product Code

• FED: Endoscopic Access Overtube, Gastroenterology-Urology

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

On-Brand Devices [PINPOINT PAQ®]

• 00858701006186: PP9050
• 10858701006237: PP9096
• 10858701006176: PP9031
• 10858701006220: PP9092