Atrium

GUDID 20650862199189

CONNECTOR (3/16 in X 3/8 in)

Atrium Medical Corporation

Non-ISO80369-standardized small-bore linear connector, single-use

• Primary Device ID: 20650862199189
• NIH Device Record Key: d5cf5d52-77b5-46aa-aaad-fa2991a68fc4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Atrium
• Version Model Number: 19918
• Company DUNS: 051798999
• Company Name: Atrium Medical Corporation
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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	00650862199185 [Primary]
GS1	20650862199189 [Package]; Contains: 00650862199185; Package: [25 Units]; In Commercial Distribution

FDA Product Code

• KDQ: Bottle, Collection, Vacuum

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: 2026-02-18
• Device Publish Date: 2026-02-10

On-Brand Devices [Atrium]

• 20650862199189: CONNECTOR (3/16 in X 3/8 in)
• 20650862199158: CONNECTOR (1/4 in X 1/4 in)
• 00650862199109: Connector Cap