Q2 Multiport Extension Set

GUDID 20634624952014

QUEST MEDICAL INC

Intravenous administration tubing extension set

• Primary Device ID: 20634624952014
• NIH Device Record Key: 7698b91a-b580-4443-ac83-5f6c0aaa8989
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Q2 Multiport Extension Set
• Version Model Number: 9520S
• Company DUNS: 041810693
• Company Name: QUEST MEDICAL 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00634624952010 [Primary]
GS1	20634624952014 [Package]; Contains: 00634624952010; Package: [50 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K162304

FDA Product Code

• FPA: Set, Administration, Intravascular

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-03-22
• Device Publish Date: 2021-03-12

On-Brand Devices [Q2 Multiport Extension Set]

• 20634624957125: 95712
• 00634624952003: 9520
• 20634624952014: 9520S