Q2 Multiport Extension Set 9520

GUDID 00634624952003

QUEST MEDICAL INC

Intravenous administration tubing extension set

• Primary Device ID: 00634624952003
• NIH Device Record Key: ed79f673-9ec6-42cc-9fd0-b78151cb34b4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Q2 Multiport Extension Set
• Version Model Number: 9520
• Catalog Number: 9520
• 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

Customer Support Contacts

• Phone: 800-627-0226
• Email: Custserv@questmedical.com
• Phone: 800-627-0226
• Email: Custserv@questmedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00634624952003 [Primary]
GS1	20634624952007 [Package]; Package: Shipper [50 Units]; In Commercial Distribution

FDA Product Code

• FPA: Set, Administration, Intravascular

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-06-07

On-Brand Devices [Q2 Multiport Extension Set]

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