A-Line

GUDID 30889483613119

3cc A-Line 23g x 1" Q-Cork, 25u BH

SUNMED, LLC

Arterial blood sampling kit Arterial blood sampling kit Arterial blood sampling kit Arterial blood sampling kit Arterial blood sampling kit Arterial blood sampling kit Arterial blood sampling kit Arterial blood sampling kit Arterial blood sampling kit Arterial blood sampling kit Arterial blood sampling kit Arterial blood sampling kit Arterial blood sampling kit Arterial blood sampling kit Arterial blood sampling kit Arterial blood sampling kit Arterial blood sampling kit Arterial blood sampling kit

• Primary Device ID: 30889483613119
• NIH Device Record Key: fcef8492-08f5-41f7-bc25-6c2d4f3232a5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: A-Line
• Version Model Number: 3300-26-S
• Company DUNS: 069009268
• Company Name: SUNMED, LLC
• 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: true
• 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	10889483613115 [Primary]
GS1	30889483613119 [Package]; Contains: 10889483613115; Package: [100 Units]; In Commercial Distribution

FDA Product Code

• CBT: Arterial Blood Sampling Kit

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: 2024-05-27
• Device Publish Date: 2024-05-17

On-Brand Devices [A-Line]

• 30889483613119: 3cc A-Line 23g x 1" Q-Cork, 25u BH
• 30889483613102: 3cc A-Line 22g x 1" Safety Tip™, 50u BH
• 30889483613096: 3cc A-Line 23g x 1" SafetyTip™, 50u BH