Q2 IV Administration Set

GUDID 20634624101306

QUEST MEDICAL INC

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• Primary Device ID: 20634624101306
• NIH Device Record Key: 3d47d2a5-e110-4d35-91e1-6297a3f6ae01
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Q2 IV Administration Set
• Version Model Number: ASV10130
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00634624101302 [Primary]
GS1	20634624101306 [Package]; Contains: 00634624101302; Package: [50 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K213588

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: 2022-12-14
• Device Publish Date: 2022-12-06

On-Brand Devices [Q2 IV Administration Set]

• 20634624901036: ASV103Y
• 00634624901025: ASV102Y
• 00634624901018: ASV101Y
• 20634624601257: ASV60125
• 20634624101306: ASV10130
• 20634624101252: ASV10125
• 20634624101153: ASV10115