A-Line

GUDID 30889483613102

3cc A-Line 22g x 1" Safety Tip™, 50u BH

SUNMED, LLC

Arterial blood sampling kit

• Primary Device ID: 30889483613102
• NIH Device Record Key: 79873435-cb07-45bc-a7c0-b9de0c3cfbf5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: A-Line
• Version Model Number: 3332-91-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	10889483613108 [Primary]
GS1	30889483613102 [Package]; Contains: 10889483613108; 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