PINPOINT PAQ®

GUDID 10858701006220

Novadaq Technologies Inc

Laparoscopic surgical procedure kit, medicated

• Primary Device ID: 10858701006220
• NIH Device Record Key: 5e2971b4-380d-468c-acc6-6327a8bee371
• Commercial Distribution Discontinuation: 2023-10-27
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: PINPOINT PAQ®
• Version Model Number: PP9092
• 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	10858701006220 [Primary]
GS1	20858701006227 [Package]; Package: box [10 Units]; Discontinued: 2023-10-27; Not 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: 2023-10-30
• Device Publish Date: 2016-09-23

On-Brand Devices [PINPOINT PAQ® ]

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